Back to search

Article

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

2022-03-27

Abstract excerpt

Single-cell DNA sequencing (scDNA-seq) has enabled the identification of single nucleotide somatic variants and the reconstruction of cell phylogenies. However, statistical phylogenetic models for cell phylogeny reconstruction from raw sequencing data are still in their infancy. Here we present SIEVE (SIngle-cell EVolution Explorer), a statistical method for the joint inference of somatic variants and cell phyloge...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
9f450907-e4cd-529b-9087-043a87bc9f00
DOI
10.1101/2022.03.24.485657
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing dataDOI 10.1101/2022.03.24.485657
Select a neighboring publication to make it the new centre.