Back to search

Article

xAtlas: Scalable small variant calling across heterogeneous next-generation sequencing experiments

2018-04-05

Abstract excerpt

<h4>Motivation</h4> The rapid development of next-generation sequencing (NGS) technologies has lowered the barriers to genomic data generation, resulting in millions of samples sequenced across diverse experimental designs. The growing volume and heterogeneity of these sequencing data complicate the further optimization of methods for identifying DNA variation, especially considering that curated highconfidence v...

Topics

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

Identifiers and source

Literature Corpus work
25b924b3-4b58-55a2-a07c-197ca13b3ef6
DOI
10.1101/295071
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.
xAtlas: Scalable small variant calling across heterogeneous next-generation sequencing experimentsDOI 10.1101/295071
Select a neighboring publication to make it the new centre.