CCGE-BOADICEA / pedigreejsLinks
A web tool for building pedigrees, https://ccge-boadicea.github.io/pedigreejs/
☆68Updated 2 weeks ago
Alternatives and similar repositories for pedigreejs
Users that are interested in pedigreejs are comparing it to the libraries listed below
Sorting:
- Pedigree drawing with ease☆24Updated 3 years ago
- Website to analyze conflicting assertions in ClinVar☆19Updated last week
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- myVCF: a web-based platform for target and exome mutations data management☆20Updated 4 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 6 years ago
- An online pedigree tool for research applications. Build pedigrees interactively and store as images or text files in ped format. QuickPe…☆30Updated 3 months ago
- Example project for integrating igv.js and flask☆26Updated 8 months ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆34Updated 2 months ago
- PharmGKB NGS Pipeline☆19Updated 7 years ago
- Genomic VCF to tab-separated values☆48Updated 2 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Updated 4 years ago
- Phenotype driven gene prioritization for HPO☆51Updated 4 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- Streamlined duo/trio analysis and pedigree haplotyping: from VCF to interactive HTML☆15Updated last year
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated last month
- Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products☆36Updated 2 months ago
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Updated 6 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆38Updated 5 years ago
- Generic human DNA variant annotation pipeline☆59Updated last year
- TREDPARSE: HLI Short Tandem Repeat (STR) caller☆25Updated 5 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- ☆33Updated 4 years ago
- ☆28Updated 8 years ago
- (WIP) best-practices workflow for rare disease☆62Updated last year
- Data visualization and analysis framework focused on phenotype-molecular data integration at cohort level.☆47Updated this week
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆57Updated this week
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆51Updated this week
- mtDNA Variant Caller☆35Updated last year
- A method to identify structural variation from sequencing data in target regions☆32Updated 5 years ago
- OLD REPOSITORY - Go to☆31Updated 7 years ago