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Are you looking to sequence a bunch of samples from a wild population in low-coverage but don't have a reference panel? You might be surprised how well it can work. See for yourself in our new benchmark study: doi.org/10.1093/molb...
Abstract. Whole genome sequencing (WGS) of a large number of samples is costly. Solutions include targeting a proportion of the genome (eg SNP arrays) or l
doi.org
Benchmarking imputation accuracy in the presence or absence of a reference panel
1mo
Alexandros Topaloudis