mvelinder / ped_drawLinks
Pedigree drawing with ease
☆23Updated 3 years ago
Alternatives and similar repositories for ped_draw
Users that are interested in ped_draw are comparing it to the libraries listed below
Sorting:
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- PGxPOP☆17Updated 2 years ago
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated last week
- smCounter: a versatile UMI-aware variant caller to detect both somatic and germline SNVs and indels. Published in article "Detecting very…☆20Updated 6 years ago
- ☆41Updated 9 months ago
- VEP Plugin to annotate high-impact five prime UTR variants☆27Updated 10 months ago
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆33Updated last month
- TIDDIT - structural variant calling☆73Updated 2 months ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 4 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- A variant caller for the GBA gene using WGS data☆22Updated 10 months ago
- Variant caller GUI + genetic disease analysis☆22Updated 5 years ago
- Structural Variant Index☆74Updated 6 months ago
- Python package and routines for merging VCF files☆29Updated 4 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆29Updated 11 months ago
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- heuristics to merge structural variant calls in VCF format.☆36Updated 8 years ago
- mtDNA Variant Caller☆34Updated 6 months ago
- Snakemake-based workflow for detecting structural variants in genomic data☆80Updated 4 months ago
- ☆12Updated 11 months ago
- Detection of CNVs (deletion/duplication) in target panel based NGS data☆16Updated 2 years ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆34Updated 8 years ago
- ☆39Updated last year
- an empirical Bayesian framework for mutation detection from cancer genome sequencing data☆31Updated 9 years ago
- Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of func…☆28Updated last year
- ☆22Updated 2 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆56Updated 7 years ago
- Read visualizer for structural variants☆84Updated 6 years ago