HIGHLIGHTS
- who: Marcin Kierczak from the for Life Laboratory Uppsala University have published the Article: Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability, in the Journal: NATURE COMMUNICATIONS NATURE COMMUNICATIONS of 15/06/2021
- what: The majority of studies aiming to investigate the effect of rare variants share the common approach of using a test that collapses the effects of multiple genetic variants. The authors are analysing SNVs and indels, identified by high coverage WGS, in relation to the protein expression levels of 414 plasma_proteins (Supplementary Data 1). The . . .
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