
Reading Passage Question
We may not much like the fact, but we are 99.9 percent identical. This is because 99.9 percent of our DNA is common to every person, and the Human Genome Project is rightly celebrated for sequencing it. But what of the remaining 0.1 percent? It is far more significant than one might assume because if it was not for this minute percentage there would be no individual differences. We would be clones. These variations in the human code account for all individual idiosyncrasies. They are responsible for the differences between ethnic and racial groups. Perhaps most interesting of all, they also explain why some of us enjoy good health while others are more susceptible to many common diseases. It is thought that the mapping of the remaining 0.1 percent of human DNA will hasten the identification of new ways to treat common ailments such as obesity, cancer, and heart disease. The work will prove particularly useful in the search for new diagnostic tests, the customizing of treatments to best suit an individual’s genetic code, and ultimately the development of new drugs that target the DNA linked to a particular disease. The task of charting the inherited differences in the human genome has fallen to 200 scientists drawn from nine countries across every (populated) continent. They will screen people drawn from all the major human populations.
“We May Not Much Like the Fact, But We are 99.9 Percent Identical” is a GMAT reading comprehension passage with answers. Candidates must have a solid grip in English GMAT reading comprehension. There are 5 multiple choice questions in the above GMAT Reading Comprehension passages. GMAT Reading Comprehension Questions are delineated to evaluate candidates’ abilities to analyze and be conceptual for the answers. Candidates can brace up and take preparation by answering GMAT Reading Comprehension Practice Questions.
Solution and Explanation
Q1. In the context of the passage the word sequencing refers to:
Answer: D
Explanation: The passage mentions that we might not like the fact, but we are 99.9 percent the same. It states that 99.9 percent of our DNA is familiar to every person. Henceforth, the Human Genome Project is rightly celebrated for sequencing it. The word sequencing therefore refers to the work of the Human Genome Project. Therefore, option(D) is an applicable answer against the above question.
Q2. Which of the following topics is not touched upon in the passage?
Answer: D
Explanation: The passage states that the work will prove useful in the search for new diagnostic tests. It also mentions the customization of treatments for the benefit of the genetic code of an individual. However, in spite of this, the concern of preventative therapies was not mentioned in the passage. So, option(D) stands fit for this above question.
Q3. It can be inferred that the work will:
Answer: A
Explanation: The work, as mentioned in the passage, proves very beneficial in the search for new diagnostic tests and customized treatments. It has been used to suit an individual’s genetic code, and ultimately to develop new drugs. It thereby targets the DNA which are interconnected to a particular disease. The search for genes which participate in causing the common diseases can be inferred from the passage. Therefore, option(A) fits to be justified for this question.
Q4. In reaching the conclusion that some of us enjoy good health while others are more susceptible to many common diseases, the author relies on which premise?
Answer: B
Explanation: It is mentioned in the passage about the differences in the human code narrates about all respective idiosyncrasies. They are liable for the contrasts between ethnic and racial groups. Although mainly, they also elaborated a reason. They mention the reason why some of us enjoy good health at the time when others are likely to be influenced by many common diseases. Thus, option(B) is the right choice.
Q5. Which of the following questions are not answered in the passage?
Answer: E
Explanation: The passage describes that the mapping will manage new treatments. Nevertheless, how these new treatments will be possible through the genetic differences sequencing was not mentioned by the narrator in the passage. The procedure of mapping the remaining 0.1 percent of DNA helps for diagnostic tests, customized treatments and new drugs was not mentioned. Thus, option(E) will be the correct statement in regards to this question.
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