Back to search

Article

Integer programming framework for pangenome-based genome inference

2024-10-29

Abstract excerpt

Affordable genotyping methods are essential in genomics. Commonly used genotyping methods primarily support single nucleotide variants and short indels but neglect structural variants. Additionally, accuracy of read alignments to a reference genome is unreliable in highly polymorphic and repetitive regions, further impacting genotyping performance. Recent works highlight the advantage of haplotype-resolved pangeno...

Topics

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

Identifiers and source

Literature Corpus work
3abe20c7-deb9-5b06-8641-cc6fe4f1814c
DOI
10.1101/2024.10.27.620212
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.
Integer programming framework for pangenome-based genome inferenceDOI 10.1101/2024.10.27.620212
Select a neighboring publication to make it the new centre.