FDA / precisionFDALinks
precisionFDA is a cloud based platform that provides an environment where the community can test, pilot, and benchmark new approaches to validating their next-generation sequencing (NGS) analysis pipelines. PrecisionFDA offers community members a secure and independent work area where, at their discretion, their bioinformatics tools or data can …
☆64Updated 4 months ago
Alternatives and similar repositories for precisionFDA
Users that are interested in precisionFDA are comparing it to the libraries listed below
Sorting:
- Documentation for the MatchmakerExchange APIs☆33Updated last year
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 2 years ago
- PharmGKB NGS Pipeline☆17Updated 6 years ago
- Predict mutated T-cell epitopes from sequencing data☆30Updated 4 months ago
- Companion repo for ExAC paper, 2015☆33Updated 8 years ago
- Machine Learning to Detect Cancer Biomarkers from RNAseq Data☆34Updated 5 years ago
- Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data☆87Updated 4 years ago
- TCGAbiolinksGUI code development for R/Bioconductor submission http://tcgabiolinks.fmrp.usp.br:3838/☆36Updated 3 years ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 6 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- CWL implementation of CloudNeo: A cloud pipeline for identifying patient-specific tumor neoantigens☆19Updated 6 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆97Updated 2 years ago
- Tutorial for working with cloud infrastructure and AWS from R☆20Updated 7 years ago
- Chart to aid in understanding mutations and their location on a gene.☆22Updated 2 years ago
- An interactive learning resource for next-generation sequencing (NGS) techniques☆29Updated 6 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 5 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆38Updated 7 years ago
- Tools for next-generation sequencing analysis☆88Updated 6 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- http://bam.iobio.io☆47Updated last year
- List of tools and resources related to the 10x Genomics GEMCode/Chromium system☆84Updated 6 years ago
- The GenePattern Server web application☆36Updated last month
- NExt generation Analysis Toolbox☆14Updated 9 years ago
- A framework for network analysis and display of SNPs☆19Updated 8 years ago
- Vials is a Caleydo Web application for visualizing alternative splicing based on mRNAseq data.☆13Updated 7 years ago
- Run bcbio-nextgen genomic sequencing analyses using isolated containers and virtual machines☆65Updated 5 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- Exploratory data analysis for pooled CRISPR/Cas9 screens☆21Updated 8 years ago