opentargets-archive / genetics-app
Open Targets Genetics UI
☆14Updated last month
Alternatives and similar repositories for genetics-app:
Users that are interested in genetics-app are comparing it to the libraries listed below
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 5 years ago
- R htmlwidget package for ideogram.js☆16Updated 2 years ago
- Add functional variant annotation to MAF file☆11Updated 4 months ago
- R function to plot high quality, elegant heatmap using 'ggplot2' graphics . Some of the important features of this package are, colorin…☆11Updated 8 years ago
- Normalization and difference calling for Next Generation Sequencing (NGS) data via joint multinomial modeling.☆11Updated 3 years ago
- stageR package☆11Updated 2 years ago
- Easily run WDL workflows on GCP☆13Updated 3 years ago
- Mostly deprecated in favor of : https://github.com/hbc/bcbioRNASeq. Quality control, differential gene/transcript expression and pathway …☆24Updated 7 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 5 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- integrative pathway analysis with modern PCA methodology and gene selection☆11Updated last year
- Library for indexing VCF files for random access searches by rsID☆17Updated last year
- Examples of kallisto + sleuth☆11Updated 7 years ago
- Computable build reports, package metadata, and download stats from the Bioconductor project☆21Updated 2 weeks ago
- Allele frequency filter app☆14Updated 2 years ago
- Scripts for generating integrated dataset from publically available data sources to evaluate known genetic associations evidence of varyi…☆11Updated 4 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- A tool to examine duplicate read characteristics in a BAM file☆12Updated 7 years ago
- ☆11Updated 6 years ago
- Allele-Specific Quantification of Structural Variations in Cancer Genomes☆17Updated 6 years ago
- R package to quickly obtain count vectors from indexed bam files☆15Updated 3 years ago
- The vignette provided has a basic sketch of the steps we interactively will go through to build a package with devtools, explains version…☆11Updated 4 years ago
- IMSEQ - IMmunogenetic SEQuence Analysis☆15Updated 6 years ago
- Fast API server for calculating linkage disequilibrium☆18Updated last year
- Data management of large-scale whole-genome sequence variant calls using GDS files (Development version only)☆45Updated last week
- An R package to increase interpretability of genes and SNPs (eg identified from GWAS and eQTL mapping)☆10Updated 2 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Updated 5 years ago
- The official Inferelator repository maintained by current or former Bonneau lab members☆9Updated 7 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 8 years ago
- Repository for signature genes from Immune Cell Atlas☆18Updated 5 years ago