CCGE-BOADICEA / pedigreejs
A web tool for building pedigrees, https://ccge-boadicea.github.io/pedigreejs/
☆65Updated last month
Alternatives and similar repositories for pedigreejs
Users that are interested in pedigreejs are comparing it to the libraries listed below
Sorting:
- An online pedigree tool for research applications. Build pedigrees interactively and store as images or text files in ped format. QuickPe…☆23Updated 3 months ago
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- HTML5 pedigree/haplotype explorer, featuring a rich selection of comparison tools.☆9Updated 4 years ago
- CN-Learn☆29Updated 5 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆64Updated last year
- TREDPARSE: HLI Short Tandem Repeat (STR) caller☆25Updated 4 years ago
- Pedigree drawing with ease☆23Updated 3 years ago
- JBrowse plugin for methylation related things☆15Updated 6 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- ☆16Updated 3 years ago
- Snakemake-based workflow for detecting structural variants in genomic data☆80Updated 3 months ago
- Structural Variant Prediction Viewer☆34Updated 7 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- Thousand Variant Callers Project Repository☆72Updated 5 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆28Updated 3 weeks ago
- mtDNA Variant Caller☆34Updated 4 months ago
- for visual evaluation of read support for structural variation☆52Updated 11 months ago
- Call regions of homozygosity and make tentative UPD calls☆11Updated 5 months ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- NovoGraph: building whole genome graphs from long-read-based de novo assemblies☆45Updated 4 years ago
- Script to convert GTC/BPM files to VCF☆46Updated 8 months ago
- Read visualizer for structural variants☆83Updated 6 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Workflows for processing RNA data for germline short variant discovery with GATK (v3+v4) and related tools☆51Updated 5 years ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆32Updated last week
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- A suite of tools for detecting expansions of short tandem repeats☆80Updated last year
- Streamlined duo/trio analysis and pedigree haplotyping: from VCF to interactive HTML☆15Updated 6 months ago