mvelinder / ped_draw
Pedigree drawing with ease
☆22Updated 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
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 4 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆25Updated last month
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- ☆23Updated 6 years ago
- An information model for representing variant annotations.☆18Updated this week
- VEP Plugin to annotate high-impact five prime UTR variants☆27Updated 6 months ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆33Updated 7 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- Transcript versions for HGVS libraries☆29Updated last month
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆45Updated this week
- ☆39Updated 5 months ago
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- ☆30Updated 4 years ago
- TIDDIT - structural variant calling☆74Updated last month
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆16Updated 9 months ago
- ☆23Updated 2 months ago
- Genomic VCF to tab-separated values☆48Updated last year
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆61Updated last year
- Generic human DNA variant annotation pipeline☆58Updated last year
- Example project for integrating igv.js and flask☆26Updated 5 months ago
- ☆9Updated 4 months ago
- ☆23Updated 5 years ago
- ☆46Updated 5 years ago
- Public repository for VariantValidator project☆73Updated this week
- smCounter: a versatile UMI-aware variant caller to detect both somatic and germline SNVs and indels. Published in article "Detecting very…☆20Updated 5 years ago
- ☆11Updated 3 weeks ago
- SV detection from paired end reads mapping☆38Updated 14 years ago
- RNAseq pipeline for alternative splicing junctions☆12Updated 7 months ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆22Updated last year