Griffan / VerifyBamIDLinks
VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
☆99Updated 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☆81Updated last year
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆103Updated 4 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆72Updated last year
- ABRA2☆92Updated 2 years ago
- A tool for profiling long STRs from short reads☆99Updated 4 years ago
- A suite of tools for detecting expansions of short tandem repeats☆83Updated 2 years ago
- Tools for processing and analyzing structural variants.☆154Updated 3 years ago
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago
- WisecondorX — An evolved WISECONDOR☆103Updated last month
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 3 years ago
- BAM Statistics, Feature Counting and Annotation☆150Updated last week
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆82Updated 2 years ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆49Updated last year
- don't get DUP'ed or DEL'ed by your putative SVs.☆106Updated 4 years ago
- Toolkit for calling structural variants using short or long reads☆109Updated 2 weeks ago
- Bayesian genotyper for structural variants☆134Updated 4 years ago
- phasing and Allele Specific Expression from RNA-seq☆116Updated last year
- Scalable gVCF merging and joint variant calling for population sequencing projects☆170Updated last year
- Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data☆114Updated 3 years ago
- SV caller for nanopore data☆92Updated 5 years ago
- ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.☆74Updated 3 months ago
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆90Updated 3 weeks ago
- Data and information about the Polaris study☆53Updated 5 years ago
- Visualization and annotation of CNVs from population-scale whole-genome sequencing data☆72Updated 7 years ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆159Updated 7 months ago
- NEAT read simulation tools☆101Updated 3 years ago
- ☆91Updated 3 years ago
- software tools for haplotype assembly from sequence data☆222Updated 8 months ago
- Read visualizer for structural variants☆84Updated 7 years ago
- Graph realignment tools for structural variants☆162Updated 2 years ago