The method trick is calling SNVs from scRNA-seq, Gavin Wilson et al solved this in 2021, see in @GenomeBiology & the part we solved was to find good filter set to call enough mutations to build good enough cell trees, thx 4 scSNV consultation, Gavin 6
RT @GenomeBiology: scSNV, from, @jonyeung and co, a method for identifying variants in droplet scRNA-seq data. It takes advantage of molecu…
RT @BioDecoded: scSNV: accurate dscRNA-seq SNV co-expression analysis using duplicate tag collapsing | Genome Biology https://t.co/N5gOejeu…
RT @BioDecoded: scSNV: accurate dscRNA-seq SNV co-expression analysis using duplicate tag collapsing | Genome Biology https://t.co/N5gOejeu…