@jim_bo_ GenCove is the only commercial implementation I know of, doing very accurate imputation from 0.4x (https://t.co/wCLVfWU5ec). We impute from OncoPanel at 0.04x; BGI did it from NIPTs of 0.06-0.1x (https://t.co/RpVHjdntwL).
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5,042 followers
Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics. #NGS #Pharmacogenetics https://t.co/NmO0hYIHQt #BMCgenomics
1,875 followers
Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics https://t.co/qwVzpJubv8
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RT @doctorveera: Low pass sequencing at 0.4x is as good as genotyping arrays. Increasing the coverage slightly higher yields better perform…