srbehera / FixItFelixLinks
☆23Updated 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.☆36Updated 2 years ago
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆38Updated 9 months ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆39Updated 2 months ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆38Updated last month
- heuristics to merge structural variant calls in VCF format.☆38Updated 9 years ago
- Variant annotation and merging pipeline☆41Updated 6 months ago
- ☆44Updated last year
- Structural variant (SV) analysis tools☆40Updated last year
- ☆35Updated 4 years ago
- Structural variant benchmark☆21Updated 10 months ago
- Pipeline for structural variant image curation and analysis.☆49Updated 4 years ago
- MethPhaser: methylation-based haplotype phasing of human genomes☆52Updated 10 months ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 5 months ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Updated 2 years ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Updated 3 years ago
- Joint structural variant and copy number variant caller for HiFi sequencing data☆69Updated 2 months ago
- ☆51Updated last year
- Sample Contamination Estimate from VCF☆20Updated last year
- Population-wide Deletion Calling☆35Updated 9 months ago
- Structural Variant Index☆75Updated last year
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆54Updated 10 months ago
- ☆33Updated 3 years ago
- Structural variant merging tool☆57Updated last year
- DEPRECATED - Workflow for the comprehensive detection and prioritization of variants in human genomes with PacBio HiFi reads☆39Updated 2 years ago
- ☆84Updated 10 months ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- ☆23Updated 8 months ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- Working space for the GIAB TR benchmarking project☆23Updated last year
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆48Updated 5 years ago