DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
tumor
cancer-genomics
germline
structural-variation
svs
delly-users
genomic
rearrangement
delly
sv-discovery
-
Updated
Mar 1, 2024 - C++
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
Structural variant VCF annotation, duplicate removal and comparison
A tutorial on structural variant calling for short read sequencing data
A workflow for using SpeedSeq to align and call SVs from WGS data
Add a description, image, and links to the delly topic page so that developers can more easily learn about it.
To associate your repository with the delly topic, visit your repo's landing page and select "manage topics."