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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 ...
Using STING-seq, short for systematic targeting and inhibition of noncoding GWAS loci with single cell sequencing, Sanjana and his team identified promising sequence variants linked to various ...
Functional Characterization of Variants of Unknown Significance of Fibroblast Growth Factor Receptors 1-4 and Comparison With AI Model–Based Prediction An economic model was developed to estimate the ...
The non-coding genome, once dismissed as "junk DNA", is now recognized as a fundamental regulator of gene expression and a key player in understanding complex diseases. Following the landmark ...
AMSTERDAM--(BUSINESS WIRE)--Annogen, the Amsterdam based biotech company behind the SuRE™ technology for the functional annotation of the non-coding part of the genome, today announced it has begun a ...
A new study has revealed the case for more extensive gene mapping in disease research, with whole genome sequencing offering an unprecedented look at the makeup and behavior of Hodgkin lymphoma that ...
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