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:
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated last month
- simple comparison of snakemake, nextflow and cromwell/wdl☆49Updated 4 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆34Updated last week
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- TIDDIT - structural variant calling☆73Updated last month
- ☆40Updated 8 months ago
- Variant Interpretation Pipeline☆39Updated this week
- Mutation Identification Pipeline. Read the latest documentation:☆44Updated last year
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆29Updated 10 months ago
- Data and information about the Polaris study☆53Updated 5 years ago
- ☆25Updated 6 months ago
- Structural Variant Index☆74Updated 5 months ago
- ☆11Updated last month
- for visual evaluation of read support for structural variation☆54Updated last year
- PGxPOP☆17Updated 2 years ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Updated 2 years ago
- Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research☆29Updated this week
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆32Updated last month
- ☆12Updated 10 months ago
- VEP Plugin to annotate high-impact five prime UTR variants☆27Updated 9 months ago
- ☆9Updated 7 months ago
- an empirical Bayesian framework for mutation detection from cancer genome sequencing data☆31Updated 9 years ago
- v2.x of the microassembly based somatic variant caller☆23Updated last month
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- Snakemake-based workflow for detecting structural variants in genomic data☆80Updated 3 months ago
- seqcover allows users to view coverage for hundreds of genes and dozens of samples☆51Updated 4 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆56Updated 7 years ago