enasequence / webin-xml
Webin XML and JSON API.
☆12Updated last month
Alternatives and similar repositories for webin-xml:
Users that are interested in webin-xml are comparing it to the libraries listed below
- Project code for BioHackathon Europe 2024.☆21Updated 5 months ago
- GA4GH Variation Representation Python Implementation☆55Updated this week
- Galaxy Workflows maintained by the Intergalactic Workflow Commission☆33Updated this week
- machine-readable file format for genomic library sequence and structure☆120Updated last month
- A Python-based EGA download client☆98Updated 7 months ago
- C++ Library to parse Illumina InterOp files☆75Updated last month
- Extensible specification for representing and uniquely identifying biological sequence variation☆88Updated 3 weeks ago
- Tutorials, workflows, and convenience scripts for Single Cell Portal☆50Updated last year
- A collection of reusable WDL tasks. Category:Other☆86Updated this week
- UC Santa Cruz Computational Genomics Lab's Toil-based RNA-seq pipeline☆40Updated 4 years ago
- ☆30Updated this week
- This repo is for the metadata schemas associated with the HCA☆67Updated last week
- Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.☆114Updated 5 months ago
- Python biomart API☆65Updated last year
- Testing building mulled containers for multi-requirement tools.☆71Updated this week
- ENA upload tool - script your Open Data upload to the European Nucleotide Archive☆28Updated 2 weeks ago
- Workflows for converting between sequence data formats☆38Updated 3 years ago
- A collection of Python clients and accessory scripts for interacting with the Cromwell☆22Updated 2 years ago
- [Alpha] Janis: an open source tool to machine generate type-safe CWL and WDL workflows☆43Updated last year
- Data Science Operations (dso) command line tool☆31Updated this week
- Module for embedding igv.js in an IPython notebook☆74Updated 2 months ago
- a Medical Genetics Sequence Analysis Pipeline☆82Updated this week
- A simple pythonic interface to biomart.☆55Updated 5 years ago
- Read specialized NGS formats as data frames in R, Python, and more.☆70Updated last week
- BaseSpace Python SDK☆37Updated 3 years ago
- A proof of concept of RNAseq pipeline☆77Updated this week
- MyVariant.info: A BioThings API for human variant annotations☆94Updated last week
- Parse Illumina sample sheets with Python☆50Updated last year
- Central repository for the VICC metakb web application☆15Updated this week
- An information model for representing variant annotations.☆18Updated this week