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Read the passage carefully and answer the following questions:
It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.
Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.
One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.
And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.
Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”
Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents' concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.
Q. Hilliard likens Genomics to nuclear fusion for which one of the following reasons?
  • a)
    Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.
  • b)
    Like nuclear fusion, the benefits of genomics are not equally available to all countries.
  • c)
    Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental. 
  • d)
    Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion. 
Correct answer is option 'C'. Can you explain this answer?
Most Upvoted Answer
Read the passage carefully and answer the following questions:It&rsquo...
Options A, B and D require extraneous information and hence cannot be concluded from the passage. The passage does not discuss the potential effects of nuclear fusion on minorities or its penetration in various countries, or the human capital required. 
The author presents the benefits that genomics could bring about and also discusses Hilliard's response to concerns over the potential misuse of the results obtained. {Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid}. Hillard further remarks that, "Genomics, like nuclear fusion, can be weaponized and dangerous". This brings out the other side of the story. 
Hence, option C is the answer.
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Community Answer
Read the passage carefully and answer the following questions:It&rsquo...
Explanation:

Genomics and Nuclear Fusion Comparison:
- Hilliard likens genomics to nuclear fusion because both are considered double-edged swords, meaning they have the potential to bring both benefits and risks.
- Just like nuclear fusion can be harnessed for energy production but also for destructive purposes, genomics can be used for medical advancements but also has the potential for misuse.

Genomics as a Double-Edged Sword:
- Genomics, like nuclear fusion, has the power to transform healthcare by enabling precision medicine tailored to individuals' genetic makeup.
- However, genomics also raises ethical concerns such as privacy, discrimination, and potential misuse of genetic information.

Benefits and Risks:
- The comparison to nuclear fusion highlights that while genomics offers tremendous potential for improving healthcare outcomes, it also poses risks if not used responsibly.
- It serves as a cautionary reminder that advancements in genomics must be accompanied by ethical considerations and safeguards to prevent harm.

Conclusion:
- In essence, Hilliard's comparison underscores the need for careful and responsible use of genomics to maximize its benefits while mitigating potential risks, similar to how nuclear fusion requires precise control to harness its power effectively.
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Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q."But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people." Which of the following cannot be inferred from the statement?

Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Which of the following statements is Constance Hilliard least likely to agree with?

Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.The central point in the fifth paragraph is that

'Aashapurna housing society' has apartments in two wings: east wing and west wing. On occasion of Christmas there is a get-together event being organized by the working committee (WC) of the society. An event comprising a quiz competition, a dumb charades game and a spin the bottle game is to take place, but since all residents of society cannot participate, a pre-final event within the east and west wings takes place separately and selected participant out of these events would compete in final against each other. Secretary of east wing of society supervises the games within his wing and allows each resident to take part in only one game of their choice. All participants of quiz contest are asked 50 questions each and get 1 point for 1 correct answer and 0 point for a wrong answer. All participants of dumb charade are given 50 chances to guess names of 50 movies, and get 1 point for 1 correct guess provided they do not guess a wrong movie name, after which they are considered out of game. Each participant of spin the bottle play 50 rounds of game together and winner of each round gets 1 point and others get 0 point. So, if there are 'n' number of participants then we get '50n' rounds. The game is based on sheer chance. After all games are conducted, the points distribution for East wing residents for quiz competition turned out to be as given below. The similar score was observed for the other two games as well.Answer following questions based on the above information, considering that the following questions are for the final rounds that are to be conducted:A team comprising of 10 participants is to be selected for spin the bottle, what should be the criteria for selection of the team to make sure best participants get selected?

In the 2006 Common Wealth games, there was participation from five different countries - USA, China, UK, Australia and Japan. From each of these five countries there were athletes participating in one of the five following events: shot put, javelin, high jump, long jump and marathon. Each participant was allowed to participate in exactly one of the five events.Further it is known that there were at least two participants and at most ten participants from each country and the total number of participants from all the five countries put together was a perfect square.The following information is also available:I. The number of participants in javelin was exactly half the number of participants in each of the other events.II. USA sent an equal number of participants in shot put, high jump and long jump.III. The maximum number of participants sent by Japan is for the long jump event and each country sent at least one participant for the long jump and shot put events.IV. The number of participants from China was two more than that from USA, which in turn was one more than that from UK, which in turn was one more than that from Australia which in turn was one more than that from Japan.V. Except Japan, all the other countries sent at least one participant for the javelin event while Japan sent at least one participant in each of the remaining events.VI. The number of participants sent by China for each of the events was different and there were no participants from China for the high jump event.VII. The number of participants in the marathon event sent by all the other countries other than China is equal.Q. How many countries did not send even a single participant in any one event?

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Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer?
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Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? for CAT 2025 is part of CAT preparation. The Question and answers have been prepared according to the CAT exam syllabus. Information about Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? covers all topics & solutions for CAT 2025 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer?.
Solutions for Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for CAT. Download more important topics, notes, lectures and mock test series for CAT Exam by signing up for free.
Here you can find the meaning of Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer?, a detailed solution for Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? has been provided alongside types of Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Read the passage carefully and answer the following questions:It’s been two decades since the Human Genome Project first unveiled a rough draft of our genetic instruction book. The promise of that medical moon shot was that doctors would soon be able to look at an individual’s DNA and prescribe the right medicines for that person’s illness or even prevent certain diseases. That promise, known as precision medicine, has yet to be fulfilled in any widespread way. True, researchers are getting clues about some genetic variants linked to certain conditions and some that affect how drugs work in the body. But many of those advances have benefited just one group: people whose ancestral roots stem from Europe. In other words, white people.Instead of a truly human genome that represents everyone, “what we have is essentially a European genome,” says Constance Hilliard, an evolutionary historian at the University of North Texas in Denton. “That data doesn’t work for anybody apart from people of European ancestry.” She’s talking about more than the Human Genome Project’s reference genome. That database is just one of many that researchers are using to develop precision medicine strategies. Often those genetic databases draw on data mainly from white participants. But race isn’t the issue. The problem is that collectively, those data add up to a catalog of genetic variants that don’t represent the full range of human genetic diversity.One solution is to make customized reference genomes for populations whose members die from cancer or heart disease at higher rates than other groups, for example, or who face other worse health outcomes, Hilliard suggests. Hilliard’s hypothesis is that precision medicine, which tailors treatments based on a person’s genetic data, lifestyle, environment and physiology, is more likely to succeed when researchers consider the histories of groups that have worse health outcomes.And the more specific the better. For instance, African Americans who descended from enslaved people have geographic and ecological origins as well as evolutionary and social histories distinct from those of recent African immigrants to the United States. Those histories have left stamps in the DNA that can make a difference in people’s health today. The same goes for Indigenous people from various parts of the world and Latino people from Mexico versus the Caribbean or Central or South America.Results of a survey conducted by Science News revealed that one big drawback to Hilliard’s proposal may be social rather than scientific. Many respondents expressed concern that even well-intentioned scientists might do research that ultimately increases bias and discrimination toward certain groups. As one respondent put it, “The idea of diversity is being stretched into an arena where racial differences will be emphasized and commonalities minimized. The fear is that any differences that are found would be exploited by those who want to denigrate others. This is truly the entry to a racist philosophy.” Indeed, the Chinese government has come under fire for using DNA to identify members of the Uighur Muslim ethnic group, singling them out for surveillance and sending some to “reeducation camps.”Hilliard says that the argument that minorities become more vulnerable when they open themselves to genetic research is valid. “Genomics, like nuclear fusion, can be weaponized and dangerous,” she says in response to respondents concerns. “Minorities can choose to be left out of the genomic revolution or they can make full use of it,” by adding their genetic data to the mix.Q.Hilliard likens Genomics to nuclear fusion for which one of the following reasons?a)Like nuclear fusion, genomics can be misused to target minorities and ratify human right violations.b)Like nuclear fusion, the benefits of genomics are not equally available to all countries.c)Genomics, like nuclear fusion, is a double-edged sword and could either be beneficial or detrimental.d)Genomics, like nuclear fusion, requires large human capital for research, and this human capital is often obtained through force and coercion.Correct answer is option 'C'. 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