Kur1sutaru / fantastic_databases_and_where_to_find_themLinks
Repository of databases for omic data
☆15Updated 2 years ago
Alternatives and similar repositories for fantastic_databases_and_where_to_find_them
Users that are interested in fantastic_databases_and_where_to_find_them are comparing it to the libraries listed below
Sorting:
- Run cBioPortal using Docker Compose☆20Updated this week
- Software to study why most genes are ignored☆15Updated 7 years ago
- A web application for finding and comparing bioinformatics training materials on GitHub and GitLab☆44Updated 5 months ago
- Documentation of the Snakemake-Workflows project☆155Updated 3 years ago
- Scripts and data for Plotting in R for Biologists, a video course on YouTube☆61Updated 5 years ago
- The Polygenic Score Catalog Calculator is a nextflow pipeline for polygenic score calculation☆154Updated last month
- A modular annotation tool for genomic variants☆142Updated 2 weeks ago
- GATK RNA-Seq Variant Calling in Nextflow☆137Updated 3 years ago
- Short lessons from FAS Informatics coffee hour☆155Updated 2 years ago
- Curated list of bioinformatics formats and publications☆54Updated 6 years ago
- Learning the Variant Call Format☆147Updated 5 months ago
- Curated Metagenomic Data of the Human Microbiome☆149Updated 2 months ago
- ☆77Updated 4 years ago
- Tutorials for statistical genetics short courses☆36Updated this week
- In-depth analysis of normalization and transformation methods for building coexpression networks from RNA-seq data.☆15Updated 2 years ago
- Demonstrating best practices for bioinformatics command line tools☆117Updated 5 years ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆163Updated 3 weeks ago
- Rare variant test software for next generation sequencing data☆141Updated 3 years ago
- Example Nextflow pipelines and programming techniques☆106Updated 3 months ago
- A tutorial on how to run basic polygenic risk score analysis☆84Updated 2 years ago
- Lightweight and Fast; RNA-seq quantification at the event-level☆116Updated 8 months ago
- A collection of scripts to assist in the retrieval of data from the ENA Browser☆92Updated 5 months ago
- GeneWalk identifies relevant gene functions for a biological context using network representation learning☆133Updated last year
- Automated and customizable preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workf…☆167Updated last month
- Backend Server for CIViC Project☆39Updated 2 years ago
- The Pharmacogenomic Clinical Annotation Tool☆154Updated last month
- Repository of Nextflow+BioContainers workflows☆14Updated 4 years ago
- ☆19Updated 3 years ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆86Updated 2 years ago
- deep residual neural network for classifying the pathogenicity of missense mutations.☆115Updated 4 years ago