Back to search

Article

Segpy: a streamlined, user-friendly pipeline for variant segregation analysis

2024-12-29

Abstract excerpt

Understanding the role of genetic variants in disease is essential for diagnostics and the advancement of genomic medicine. While the advent of high-throughput sequencing has been matched by the development of sophisticated genomic analysis tools, these packages often involve complex analytical procedures that can be challenging for researchers with limited computational experience. Additionally, modern genomic da...

Topics

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

Identifiers and source

Literature Corpus work
c92090b3-843d-5d32-9ded-51c0f8e76ad4
DOI
10.1101/2024.12.26.24319616
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.
Segpy: a streamlined, user-friendly pipeline for variant segregation analysisDOI 10.1101/2024.12.26.24319616
Select a neighboring publication to make it the new centre.