PacificBiosciences / pb-human-wgs-workflow-wdlLinks
☆12Updated 2 years ago
Alternatives and similar repositories for pb-human-wgs-workflow-wdl
Users that are interested in pb-human-wgs-workflow-wdl are comparing it to the libraries listed below
Sorting:
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 2 months ago
- Evaluation of phasing performance☆23Updated 7 years ago
- ☆15Updated last year
- VCF files of SVs using long-read sequencing (LRS).☆22Updated 3 years ago
- Plot CNV data with a genome viewer in R☆15Updated 8 years ago
- Structural Variation breakpoint discovery via adaptive learning☆16Updated 2 years ago
- Location of public benchmarking; primarily final results☆18Updated 8 months ago
- ☆16Updated 9 months ago
- PopSTR - A Population based microsatellite genotyper☆33Updated last year
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 7 months ago
- add true-negative SVs from a population callset to a truth-set.☆15Updated 3 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated this week
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Updated 6 years ago
- Structural variant (SV) analysis tools☆38Updated last year
- Sample Contamination Estimate from VCF☆21Updated 11 months ago
- ☆15Updated 4 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- Updated figures for "A benchmarking of WGS-based structural variant callers" paper☆27Updated 3 years ago
- Python library for simple and complex indels.☆12Updated last year
- CNV Rapid Aberration Detection And Reporting☆12Updated 4 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- ☆35Updated 4 years ago
- ☆13Updated 3 years ago
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Updated 5 years ago
- Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV…☆21Updated 5 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆12Updated 3 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆25Updated 9 years ago
- Tools to gather evidence for structural variation via breakpoint detection.☆19Updated 6 months ago
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆26Updated last year
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year