Sage-Bionetworks-Challenges / SMC-RNA-ChallengeLinks
☆9Updated 8 years ago
Alternatives and similar repositories for SMC-RNA-Challenge
Users that are interested in SMC-RNA-Challenge are comparing it to the libraries listed below
Sorting:
- Documentation and tutorials worth sharing.☆10Updated 2 years ago
- ☆11Updated 8 years ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 5 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- AC-PCA: simultaneously performs dimension reduction and adjustment for confounding variation☆14Updated 4 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- This is a short response to the 2018 RFI on NIH Strategic Plan for Data Science☆16Updated 7 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- Examples for the Google Genomics Pipelines API.☆50Updated 7 years ago
- Library for manipulating genomic variants and predicting their effects☆84Updated last year
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- ☆28Updated 6 years ago
- Archived version of RUVSeq☆8Updated 8 years ago
- qtools has helper functions to submit jobs to compute clusters (PBS on TSCC, SGE on oolite) from within Python☆21Updated last year
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 3 years ago
- SevenBridges Python Api bindings☆46Updated 5 months ago
- Survey of bioinformatics field☆26Updated 13 years ago
- Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆31Updated 7 years ago
- A tool for running bioinformatics workflows locally or in the cloud.☆30Updated 5 years ago
- A python script used to annotate genomic intervals.☆18Updated 5 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- A catalogue of docker images for NGS data analysis tools☆9Updated 6 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- GWAS data analysis experiments☆24Updated 5 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- Request for comments on interchangeable bioinformatics containers☆40Updated 6 years ago
- Utilities for analyzing mutations and neoepitopes in patient cohorts☆20Updated 7 years ago
- We have moved to https://github.com/limix/limix.☆24Updated 7 years ago
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆70Updated 2 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago