DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
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Updated
Aug 23, 2024 - C++
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
3D hotspot mutation proximity analysis tool
Official code repository for JAX-CNV
Front-end web client for the GraphKB project
An improved compression tool for DNA sequences
Comparison of sequencing read mapping to pangenome graphs
This repository contains the answers for coursera 's "Command Line Tools for Genomic Data Science"
This repository contains the answers for coursera 's "Bioconductor for Genomic Data Science"
Datasets and analysis results released with the REVOLVER package for Cancer Evolution.
A tool for calculating the Burrows-Wheeler transform (BWT) in a Map-Reduce fashion on Apache Spark Framework.
The R code was developed to draw the genomic track of signals for next-generation sequencing data.
Short Sequence Rastreator allows genetic diversity analysis and preparation of input files for other softwares such as STRUCTURE, DARwin and SPAGeDi.
Package to genomic prediction focused on GE genomic models
Simulate Variants for provided genomic coordinates
An R package designed for generalized linear mixed model inference in genomic sequencing studies
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