mvelinder / ped_drawLinks
Pedigree drawing with ease
☆24Updated 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 week
- Website to analyze conflicting assertions in ClinVar☆19Updated last year
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Updated 4 years ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆18Updated last year
- Mutation Identification Pipeline. Read the latest documentation:☆47Updated this week
- VEP Plugin to annotate high-impact five prime UTR variants☆27Updated last year
- (WIP) best-practices workflow for rare disease☆62Updated last year
- Generic human DNA variant annotation pipeline☆59Updated last year
- A phenotype-based tool for variant prioritization in WES and WGS data☆39Updated 2 years ago
- BrowseVCF is a web-based application and workflow to quickly prioritise disease-causative variants in VCF files.☆47Updated 5 years ago
- TIDDIT - structural variant calling☆77Updated 7 months ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- Simple vcf parser, based on PyVCF☆47Updated 6 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- ☆29Updated 4 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆55Updated this week
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆37Updated 5 years ago
- Script to convert GTC/BPM files to VCF☆47Updated last month
- Example project for integrating igv.js and flask☆26Updated 5 months ago
- A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample☆26Updated 2 years ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Updated 2 years ago
- PGxPOP☆17Updated 2 years ago
- ☆44Updated last year
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆33Updated 2 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated last week
- Concordance and contamination estimator for tumor–normal pairs☆58Updated last year
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 3 months ago
- Browser based application for viewing bam alignments☆56Updated 8 years ago