Griffan / VerifyBamIDLinks
VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
☆97Updated last year
Alternatives and similar repositories for VerifyBamID
Users that are interested in VerifyBamID are comparing it to the libraries listed below
Sorting:
- Tools for the analysis of structural variation in genomes☆79Updated last year
- Tools for processing and analyzing structural variants.☆153Updated 3 years ago
- Toolkit for calling structural variants using short or long reads☆106Updated last month
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 3 years ago
- ABRA2☆92Updated 2 years ago
- Scalable gVCF merging and joint variant calling for population sequencing projects☆163Updated last year
- Visualization and annotation of CNVs from population-scale whole-genome sequencing data☆71Updated 7 years ago
- This repository contains information about latest release from Genome in a Bottle project☆74Updated 5 years ago
- A suite of tools for detecting expansions of short tandem repeats☆82Updated 2 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆72Updated 10 months ago
- Bayesian genotyper for structural variants☆134Updated 4 years ago
- BAM Statistics, Feature Counting and Annotation☆150Updated 3 weeks ago
- SV caller for nanopore data☆91Updated 5 years ago
- don't get DUP'ed or DEL'ed by your putative SVs.☆106Updated 4 years ago
- WisecondorX — An evolved WISECONDOR☆99Updated 2 weeks ago
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆80Updated 2 years ago
- phasing and Allele Specific Expression from RNA-seq☆116Updated last year
- Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data☆114Updated 3 years ago
- Phased assembly variant caller☆121Updated 7 months ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆49Updated last year
- A tool for profiling long STRs from short reads☆97Updated 4 years ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆154Updated 4 months ago
- SV detection tool for nanopore sequence reads☆92Updated 3 months ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆78Updated last year
- A simple toolset for BED files (warning: CLI may change before bedtk becomes stable)☆140Updated last month
- A tool for somatic structural variant calling using long reads☆138Updated last week
- Jasmine: SV Merging Across Samples☆217Updated 6 months ago
- ☆39Updated last year
- The DevNet project on github stores the PacBio DevNet website.☆116Updated 7 years ago
- Data and information about the Polaris study☆53Updated 5 years ago