GMOD / ChadoLinks
the GMOD database schema
☆42Updated last year
Alternatives and similar repositories for Chado
Users that are interested in Chado are comparing it to the libraries listed below
Sorting:
- Minimum Information about any (X) Sequence” (MIxS) specification☆53Updated this week
- An information model for representing variant annotations.☆22Updated this week
- Collect of SO Ontologies☆101Updated last month
- GA4GH Variation Representation Python Implementation☆60Updated this week
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated 2 months ago
- non-redundant, compressed, journalled, file-based storage for biological sequences☆47Updated last month
- Get, parse, and extract information from the SRA metadata files☆45Updated 3 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated 3 months ago
- ☆30Updated last month
- OHMI: The Ontology of Host-Microbiome Interactions☆12Updated 3 years ago
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆70Updated last month
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- A collection of reusable WDL tasks. Category:Other☆88Updated last month
- Open-source opinionated Galaxy-based framework for microbiota analysis☆14Updated 4 years ago
- Python Phenopacket Tools☆15Updated last month
- A Python library for interacting with the Galaxy API☆93Updated 2 weeks ago
- Testing building mulled containers for multi-requirement tools.☆80Updated this week
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆75Updated 2 weeks ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆38Updated 2 years ago
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆62Updated this week
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated this week
- A modular annotation tool for genomic variants☆129Updated last week
- Transcript versions for HGVS libraries☆33Updated this week
- A repository for the schemas used for the Data Repository Service.☆63Updated 2 months ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆84Updated last month
- Sample search by metadata and features☆47Updated 2 years ago
- ☆19Updated this week
- TIDDIT - structural variant calling☆76Updated 6 months ago
- Galaxy Admin Training☆60Updated 10 months ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago