ga4gh / wiki
a place for GA4GH-related wiki pages
☆16Updated 7 years ago
Alternatives and similar repositories for wiki:
Users that are interested in wiki are comparing it to the libraries listed below
- CWL for GDC DNASeq workflows☆22Updated last week
- An information model for representing variant annotations.☆18Updated this week
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆27Updated 2 months ago
- Import a CWL workflow specification to Nextflow script (experimental)☆27Updated 6 years ago
- CWL implementation of CloudNeo: A cloud pipeline for identifying patient-specific tumor neoantigens☆19Updated 6 years ago
- Allele frequency filtering for Mendelian variant discovery☆17Updated 8 years ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:☆16Updated 8 months ago
- [Alpha] Janis: an open source tool to machine generate type-safe CWL and WDL workflows☆43Updated last year
- Convert CWL to WDL☆17Updated 8 years ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆34Updated 8 years ago
- hail-based pipelines for annotating variant callsets and exporting them to elasticsearch☆23Updated last week
- Opossum is a tool to pre-process RNA-seq reads prior to variant calling.☆28Updated 6 years ago
- H3ABioNet 16S rDNA diverstity analysis package☆18Updated 5 years ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆16Updated 11 months ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago
- ☆29Updated 4 years ago
- Variant caller GUI + genetic disease analysis☆22Updated 4 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 8 months ago
- Open-source opinionated Galaxy-based framework for microbiota analysis☆14Updated 4 years ago
- SEQSpark documentation☆18Updated 4 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 4 months ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆28Updated 4 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated last year
- ☆9Updated 8 years ago
- conda recipes for genomic data☆85Updated 3 years ago
- ☆38Updated 2 months ago