Illumina / akt
Ancestry and Kinship Tools
☆70Updated 2 years ago
Alternatives and similar repositories for akt:
Users that are interested in akt are comparing it to the libraries listed below
- don't get DUP'ed or DEL'ed by your putative SVs.☆104Updated 4 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆75Updated last year
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆96Updated 2 years ago
- An awk-like VCF parser☆56Updated last year
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆67Updated 5 months ago
- Read visualizer for structural variants☆81Updated 6 years ago
- Data and information about the Polaris study☆53Updated 5 years ago
- R package designed to simplify structural variant analysis☆72Updated 3 years ago
- Support Vector Structural Variation Genotyper☆58Updated 4 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆65Updated 2 years ago
- ☆39Updated 10 months ago
- Thousand Variant Callers Project Repository☆71Updated 5 years ago
- Structural Variant Index☆71Updated 2 months ago
- Comprehensive benchmark of structural variant callers☆45Updated 4 years ago
- A snakemake pipeline for SV analysis from nanopore genome sequencing☆51Updated 4 years ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆46Updated 4 years ago
- TIDDIT - structural variant calling☆74Updated last month
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆36Updated this week
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆22Updated last year
- A suite of tools for detecting expansions of short tandem repeats☆80Updated last year
- ☆78Updated 10 years ago
- R package for inferring copy number from read depth☆32Updated 2 years ago
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- A software for calculating telomere length☆68Updated 6 years ago
- Visualization and annotation of CNVs from population-scale whole-genome sequencing data☆70Updated 7 years ago
- SV detection from paired end reads mapping☆38Updated 14 years ago
- High-performance error correction for Illumina resequencing data☆69Updated 8 years ago
- A tool to benchmark mappers and different parameters within minutes☆43Updated 5 years ago
- My collection of light bioinformatics analysis pipelines for specific tasks☆72Updated 9 months ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆60Updated last year