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Whole genome sequencing reveals how much human heritability we can finally explain
Whole genome sequencing in nearly 500,000 UK Biobank participants shows that observed rare and common variants now explain ...
The National Institutes of Health established the Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium in 2021 with the goal of finding molecular diagnoses for individuals ...
Pacific Biosciences of California Inc.’s technology could rapidly increase the number of rare diseases—and their causes—identified by sequencing. Researchers at Children’s Mercy Research Institute in ...
Diagnosis sequencing is key to improving hospital ratings and rankings by industry groups like U.S. News & World Report, Leapfrog Group and Vizient. Manual processes for identifying high value cases, ...
Since slide-sequencing was developed in 2019 in the academic labs of Evan Macosko, MD, PhD, and Fei Chen, PhD, the technology has been making waves for its ease of use and high resolution. GEN covered ...
Journal of Experimental Botany, Vol. 66, No. 15 (2015), pp. 4483-4495 (13 pages) Recently, long non-coding RNAs (lncRNAs) have been shown to play critical regulatory roles in model plants, such as ...
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