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
3D hotspot mutation proximity analysis tool
Package to genomic prediction focused on GE genomic models
Comparison of sequencing read mapping to pangenome graphs
An improved compression tool for DNA sequences
Official code repository for JAX-CNV
Front-end web client for the GraphKB project
Enrichment analysis of motifs with ancient and recent CNEs
This repository contains the answers for coursera 's "Command Line Tools for Genomic Data Science"
Simulate Variants for provided genomic coordinates
A tool for calculating the Burrows-Wheeler transform (BWT) in a Map-Reduce fashion on Apache Spark Framework.
This repository contains the answers for coursera 's "Bioconductor for Genomic Data Science"
An R package designed for generalized linear mixed model inference in genomic sequencing studies
We are taking existing orthoMcl Software Written Perl and Translating it to Python
The R code was developed to draw the genomic track of signals for next-generation sequencing data.
Datasets and analysis results released with the REVOLVER package for Cancer Evolution.
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