DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
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Updated
Mar 1, 2024 - C++
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
microsatellite instability detection using tumor only or paired tumor-normal data
Single-cell copy number calling and event history reconstruction.
A long-read analysis toolbox for cancer and population genomics
Accucopy is a computational method that infers Allele-Specific Copy Number alterations from low-coverage low-purity tumor sequencing data.
Reference-free FASTQ filter for rare germline and somatic variants
Mutation Finder and Genome Comparison Toolset
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