There are no reviews yet. Be the first to send feedback to the community and the maintainers!
gridss
GRIDSS: the Genomic Rearrangement IDentification Software Suitebionix
Functional highly reproducible bioinformatics pipelinesStructuralVariantAnnotation
R package designed to simplify structural variant analysisbioshake
Bioinformatics pipelines with Haskell and Shakesv_benchmark
Comprehensive benchmark of structural variant callersPathOS
PathOS is a clinical application for filtering, analysing and reporting on NGS variantssocrates
HaveYouSwappedYourSamples
This project contains simple methods to measure sample relatedness and identify potential swaps and contaminationCanary
A fast and self-contained amplicon pipeline tool.clove
classification of higher-order structural variants from breakpoint dataCNspector
Web-based copy number browser.sv_tools
A few tools for plotting and reasoning about genomic structural variants.svaNUMT
assemble_var
A pipeline for the assembly of VAR genes from transcriptome dataVIRUSBreakend
Viral Integration Recognition Using Single Breakendsnix-workshop
svqsc
Structural Variation Quality Score CalculatorsvaRetro
Mungo
Python library for munging biological sequence and annotation dataIntroductionToGenomicsWorkshop
WEHI Masterclass Day 3: Genomicsdedumi
wgd.test
By modelling aneuploidy with interleaving branching processes we can make a decision about whether or not genome doubling occurred. We can also label each event as being pre or post GD.MHC-clogs
MHC Class I Gene Search toolLove Open Source and this site? Check out how you can help us