opentargets-archive / genetics-appLinks
Open Targets Genetics UI
☆15Updated 10 months ago
Alternatives and similar repositories for genetics-app
Users that are interested in genetics-app are comparing it to the libraries listed below
Sorting:
- R htmlwidget package for ideogram.js☆15Updated 3 years ago
- Examples of kallisto + sleuth☆11Updated 8 years ago
- ☆11Updated 7 years ago
- integrative pathway analysis with modern PCA methodology and gene selection☆11Updated 2 years ago
- Fast API server for calculating linkage disequilibrium☆20Updated 7 months ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- Add functional variant annotation to MAF file☆11Updated last year
- Interface to various variant calling formats.☆31Updated last year
- Machine learning use cases for teaching☆13Updated 8 years ago
- home of the bear's lair☆10Updated 8 years ago
- Data management of large-scale whole-genome sequence variant calls using GDS files (Development version only)☆46Updated last month
- Allele frequency filter app☆14Updated 3 years ago
- ☆14Updated last month
- Scripts for generating integrated dataset from publically available data sources to evaluate known genetic associations evidence of varyi…☆11Updated 5 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- HGNC Comparison of Orthology Predictions (HCOP)☆14Updated 7 years ago
- Computable build reports, package metadata, and download stats from the Bioconductor project☆22Updated last month
- Interactive table from gemini output☆10Updated 6 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- Tutorial for working with cloud infrastructure and AWS from R☆20Updated 8 years ago
- Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R☆32Updated 2 months ago
- Targeted and non-targeted anticancer drugs and drug regimens☆29Updated last week
- A server for maintaining high-throughput sequencing QC data☆13Updated 4 months ago
- Allele frequency filtering for Mendelian variant discovery☆18Updated 9 years ago
- Seamless navigation through combined results of set-based and network-based enrichment analysis☆21Updated 3 months ago
- R package to quickly obtain count vectors from indexed bam files☆15Updated 6 months ago
- R interface to megadepth: BigWig and BAM related utilities☆12Updated last year
- IMSEQ - IMmunogenetic SEQuence Analysis☆15Updated 7 years ago
- ☆10Updated 6 years ago