Back to search

Article

Monopogen: single nucleotide variant calling from single cell sequencing

2022-12-08

Abstract excerpt

<title>Abstract</title> <p>Distinguishing how genetics impact cellular processes can improve our understanding of variable risk for diseases. Although single-cell omics have provided molecular characterization of cell types and states on diverse tissue samples, their genetic ancestry and effects on cellular molecular traits are largely understudied. Here, we developed Monopogen, a computational tool enabling rese...

Topics

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

Identifiers and source

Literature Corpus work
8304d1f7-e65b-5436-874e-f81ca382d441
DOI
10.21203/rs.3.rs-2344391/v1
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.
Monopogen: single nucleotide variant calling from single cell sequencingDOI 10.21203/rs.3.rs-2344391/v1
Select a neighboring publication to make it the new centre.