srbehera / FixItFelixLinks
☆22Updated 2 years ago
Alternatives and similar repositories for FixItFelix
Users that are interested in FixItFelix are comparing it to the libraries listed below
Sorting:
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆57Updated 3 years ago
- ☆43Updated 10 months ago
- heuristics to merge structural variant calls in VCF format.☆36Updated 8 years ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆37Updated last year
- MethPhaser: methylation-based haplotype phasing of human genomes☆48Updated 5 months ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆33Updated 2 weeks ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆30Updated last week
- ☆35Updated 4 years ago
- ☆39Updated last year
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆30Updated 3 months ago
- Working space for the GIAB TR benchmarking project☆21Updated 9 months ago
- Variant annotation and merging pipeline☆39Updated 2 weeks ago
- ☆23Updated 2 months ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆48Updated 5 years ago
- Structural Variant Index☆75Updated 7 months ago
- ☆48Updated last year
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆32Updated 4 years ago
- Sample Contamination Estimate from VCF☆20Updated 9 months ago
- ☆32Updated 2 years ago
- My experimental tools on top of htslib. NOT OFFICIAL!!!☆56Updated last year
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)☆43Updated last month
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Updated last year
- ☆81Updated 5 months ago
- Immuological gene typing and annotation for genome assembly☆37Updated 4 months ago
- Structural variant merging tool☆53Updated 11 months ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆49Updated 5 months ago