opentargets / issuesLinks
Issue tracker for the Open Targets Platform
☆12Updated 2 months ago
Alternatives and similar repositories for issues
Users that are interested in issues are comparing it to the libraries listed below
Sorting:
- ☆25Updated 4 years ago
- Refining the impact of genetic evidence on clinical success☆26Updated last year
- Fine-mapping pipeline for Open Targets Genetics☆26Updated 3 years ago
- WIP : regular expressions for identifying and extracting values from HGVS nomenclature☆14Updated 7 years ago
- WDL plugin for pytest☆48Updated 2 years ago
- Code for classifying unstructured text to tissue ontology terms using natural language processing and machine learning.☆25Updated last year
- A R Bioconductor package for accessing MyGene.info services☆11Updated 7 years ago
- Open Targets python framework for post-GWAS analysis☆43Updated this week
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- ☆28Updated 6 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆29Updated this week
- Converts 'MultiQC' Reports into Tidy Data Frames☆18Updated last year
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- Calculate and plot distributions of genomic ranges☆26Updated 4 months ago
- R package for extracting mutation signatures from a list of somatic mutations☆37Updated 6 years ago
- Template for building a bioconductor workshop package using github actions☆21Updated 2 months ago
- Utilities for analyzing mutations and neoepitopes in patient cohorts☆20Updated 7 years ago
- GWAS gold standards repository☆38Updated last year
- PyIOmica (pyiomica) is a Python package for omics analyses.☆16Updated 3 months ago
- Library for indexing VCF files for random access searches by rsID☆17Updated last month
- Extends miniwdl to run workflows on AWS Batch & EFS☆22Updated last year
- iDEP: integrated Differential Expression & Pathway analysis☆14Updated 6 years ago
- ☆12Updated 3 months ago
- RNA-seq data comprehensive data analysis toolbox☆19Updated 2 years ago
- PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.☆15Updated 2 years ago
- Toolbox package for organizing and working with TCGA data☆28Updated 2 months ago
- The snakemake interface, currently works like a notebook (under development)☆19Updated 3 years ago
- Class materials for the NIH HPC snakemake class☆15Updated 11 months ago
- Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer☆21Updated 4 years ago
- Genepy is an open source utils package covering a range of useful functions for large scale genomics data analysis in python☆21Updated 2 years ago