Researchers have discovered 275 million new genetic variants from data shared by 250,000 participants of All of us Research Programme of NIH. This vast unexplored data will help better understand influence of જિનેટિક્સ on health and disease.
Researchers have identified over 275 million new આનુવંશિક ચલો from data shared by about 250,000 participants of અાપણે બધા Research Programme of National Institute of Health (NIH) of the USA. These ચલો were previously unreported and unexplored. Of the 275 million newly identified ચલો, nearly 4 million are in areas that may be associated with the disease risks.
Interestingly, nearly half of the genomic data are from participants with non-European આનુવંશિક background. This addresses a major diversity related limitation of other large genomic studies which had over 90% participants with European આનુવંશિક વંશ
નવું જીનોમિક માં નોંધાયેલા સંશોધકોને ડેટા ઉપલબ્ધ કરાવવામાં આવે છે સંશોધક વર્કબેન્ચ. ઘણા સંશોધકો ડેટાસેટનો ઉપયોગ કરી રહ્યા છે.
Study of these hitherto unexplored આનુવંશિક ચલો should contribute to understanding influences of જિનેટિક્સ on health and disease especially in under-studied communities with non-European ancestry.
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સોર્સ:
NIH. News releases- 275 million new આનુવંશિક variants identified in NIH precision medicine data. Posted 19 February 2024.Availalble at https://www.nih.gov/news-events/news-releases/275-million-new-genetic-variants-identified-nih-precision-medicine-data
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