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☆55Updated 2 weeks ago
- An information model for representing variant annotations.☆25Updated this week
- Collect of SO Ontologies☆101Updated 2 months ago
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated last month
- GA4GH Variation Representation Python Implementation☆60Updated last week
- OHMI: The Ontology of Host-Microbiome Interactions☆12Updated 3 years ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆39Updated 3 years ago
- non-redundant, compressed, journalled, file-based storage for biological sequences☆47Updated 2 weeks ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆31Updated last week
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Get, parse, and extract information from the SRA metadata files☆45Updated 3 years ago
- Interactive, web-based BLAST results visualization tool. Accessible at https://kablammo.wasmuthlab.org.☆67Updated 3 years ago
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆65Updated last week
- A metadata commons to store research software metadata☆44Updated last week
- Portable WDL workflows for CZ ID production pipelines☆48Updated 5 months ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated last week
- ☆20Updated 2 weeks ago
- VCF Observer is a VCF file analysis, comparison, and visualization tool.☆18Updated 10 months ago
- A modular annotation tool for genomic variants☆138Updated last week
- A collection of reusable WDL tasks. Category:Other☆88Updated 3 months ago
- The Genomic Epidemiology Application Ontology describes the genomics, laboratory, clinical and epidemiological contextual information req…☆23Updated last month
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆71Updated last month
- An easy-to-use way for running Galaxy workflows.☆20Updated 6 years ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- WDL’s and Dockerfiles for assembly QC process☆70Updated 4 months ago
- Phylo.IO JS tree viewer☆33Updated 4 months ago
- A Python package for Biopython that gives feature annotations from GenBank records a new and better life☆14Updated 9 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- Project Manager for NGS data analysis☆30Updated 2 months ago
- Website to analyze conflicting assertions in ClinVar☆19Updated last year