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 आनुवंशिकी on health and disease.
Researchers have identified over 275 million new आनुवंशिक variants from data shared by about 250,000 participants of हामी सबै संयुक्त राज्य अमेरिका को स्वास्थ्य को राष्ट्रीय संस्थान (NIH) को अनुसन्धान कार्यक्रम। यी भेरियन्टहरू पहिले रिपोर्ट नगरिएका र अन्वेषण नगरिएका थिए। 275 मिलियन नयाँ पहिचान गरिएका भेरियन्टहरू मध्ये, लगभग 4 मिलियन क्षेत्रहरूमा छन् जुन रोग जोखिमसँग सम्बन्धित हुन सक्छ।
Interestingly, nearly half of the genomic data are from participants with non-European आनुवंशिक background. This addresses a major diversity related limitation of other large genomic studies which had over 90% participants with European आनुवंशिक पूर्वज।
नयाँ जीनोमिक मा दर्ता अनुसन्धानकर्ताहरूलाई डाटा उपलब्ध गराइन्छ अनुसन्धानकर्ता कार्यक्षेत्र. धेरै शोधकर्ताहरूले डाटासेट प्रयोग गर्दैछन्।
Study of these hitherto unexplored आनुवंशिक variants should contribute to understanding influences of आनुवंशिकी on health and disease especially in under-studied communities with non-European ancestry.
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स्रोत:
NIH. News releases- 275 million new आनुवंशिक 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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