SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

RT @ewa_szczurek: Together with our CONET, which is a model for copy number evolution in cancer, and was also out recently in @GenomeBiolog…

RT @ewa_szczurek: Great news to share: Our new baby called SIEVE is out in @GenomeBiology! https://t.co/SmxflbO9OZ SIEVE is a statistical…

RT @BioDecoded: SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data | Genome Biolo…

RT @BioDecoded: SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data | Genome Biolo…