Jakarta post: Researches have found a technique to quickly assess disorders in babies. This new method, published Wednesday in the magazine Science Translation Medicine, is a proof of concept that it's possible to quickly scan a baby's entire DNA and pinpoint a disease-causing mutation in a couple of days instead of the more typical weeks as months. The study investigation to four babies said that the test could be one of the first partical fruits of the revolution in squencing an individual's entire DNA.
The idea behind the test is to take advantage of what is known about disease symptoms to narrow the search for genetic. And that is a good step in the right direction, said Dr. Joe Gray, an expert in genome analysis at Oregon Health and Science University. "It's a big genome," said Dr. Joe Gray, who was not involved with the study, "How o you know what part of it to search?"
While more research needs to be done before the test is ready for widespread use, he applauded the effort "If people don't push the envelope like this, then we won't get there," Dr. Gray Said.
Besides scanning a baby's DNA, the new method ...
shows disease symptoms
detects its physical disorders
points out its health condition
explains its physical condition
describes its physical appearance
Berdasarkan kalimat “The idea behind the test is to take advantage of what is known about disease symptoms to narrow the search for genetic” yang terdapat pada kalimat pertama di paragraf ke-2, dapat diketahui bahwa tes yang dilakukan diuntungkan dengan diketahuinya gejala-gejala penyakit untuk mempersempit ruang pencarian genetik sehingga pilihan jawaban (A) adalah yang paling tepat.
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