genometra / SNPediaRLinks
An R package to query SNPedia
☆11Updated last year
Alternatives and similar repositories for SNPediaR
Users that are interested in SNPediaR are comparing it to the libraries listed below
Sorting:
- Extends miniwdl to run workflows on AWS Batch & EFS☆22Updated last year
- Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R☆36Updated 3 years ago
- Repository for development of the genomic module of the CDM.☆23Updated 6 years ago
- A python tool for parsing pedigree files☆16Updated 8 years ago
- NExt generation Analysis Toolbox☆14Updated 9 years ago
- Visualization and charting JS library for streaming genomic data☆19Updated 9 months ago
- Python Phenopacket Tools☆15Updated last month
- [DEPRECATED] An R package for Google Genomics API queries.☆45Updated 2 years ago
- A pipeline that takes clinical notes from EHRs and generate phenotype terms, then generate ranked gene list☆37Updated 2 years ago
- Elastic, reproducible, and reusable genomic data science tools from R backed by cloud resources☆34Updated 3 years ago
- WDL plugin for pytest☆48Updated 2 years ago
- Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:☆17Updated last year
- WIP : regular expressions for identifying and extracting values from HGVS nomenclature☆14Updated 7 years ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 7 years ago
- A software toolkit for the interconversion of standard data models for phenotypic data☆15Updated last month
- Class materials for the NIH HPC snakemake class☆15Updated last year
- A collection of Python clients and accessory scripts for interacting with the Cromwell☆22Updated 2 years ago
- LEGACY repository for SODAR Core, preserved for saving review-related issues. See "sodar-core" for the up-to-date repository.☆15Updated 3 years ago
- Docker container for Illumina bcl2fastq☆11Updated last year
- hail-based pipelines for annotating variant callsets and exporting them to elasticsearch☆23Updated this week
- Framework for running bioinformatic workflows and pipelines using the Google Pipelines API as the underlying task-runner.☆12Updated 8 years ago
- R package for easy access, manipulation, and analysis of the Monarch Initiative or other KGX-formatted knowledge graphs.☆15Updated last month
- SEQSpark documentation☆18Updated 4 years ago
- The command-line interface to GGD☆42Updated 2 years ago
- Introduction to Cloud Computing for Genomics☆21Updated this week
- FAIR Genomes semantic metadata model. The core is a YAML file, which is transformed into all other desired output formats.☆13Updated 7 months ago
- Semantic Similarity in Bio-Ontologies☆17Updated 3 weeks ago
- Intersect multiple VCF files with haplotype awareness☆26Updated 4 years ago
- Exposing public genomics data via computable and searchable metadata☆13Updated last year
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆58Updated 6 years ago