eQTL-Catalogue / qtlmapLinks
Portable eQTL analysis and statistical fine mapping workflow used by the eQTL Catalogue
☆57Updated 3 months ago
Alternatives and similar repositories for qtlmap
Users that are interested in qtlmap are comparing it to the libraries listed below
Sorting:
- Enhanced version of the FastQTL QTL mapper☆71Updated 2 years ago
- HMMRATAC peak caller for ATAC-seq data☆99Updated last year
- A bioconductor package with minimalist design for drawing elegant tracks or lollipop plot☆74Updated last month
- A toolkit for QC and visualization of ATAC-seq results.☆72Updated 11 months ago
- HLA-TAPAS pipeline for HLA association and fine-mapping studies☆54Updated 2 years ago
- Matrix eQTL: Ultra fast eQTL analysis via large matrix operations☆89Updated 2 years ago
- Tutorial Website☆61Updated 4 years ago
- A tool for the calculation of RNA-editing index for RNA seq data☆45Updated 2 months ago
- RepEnrich2 is an updated method to estimate repetitive element enrichment using high-throughput sequencing data.☆41Updated 3 years ago
- A modular, containerized pipeline for ATAC-seq data processing☆61Updated 3 months ago
- This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to…☆60Updated 5 years ago
- REDItools are python scripts to investigate RNA editing at genomic scale.☆69Updated 5 months ago
- An R package for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline☆69Updated 9 months ago
- ☆49Updated 2 years ago
- MMQTL is a statistical package applying meta-analysis to detect multiple QTL signals integrating signals among conditions, with control f…☆12Updated 8 months ago
- Molecular QTL analysis protocol developed by ADSP Functional Genomics Consortium☆47Updated 3 weeks ago
- ☆63Updated 4 years ago
- Publication quality NGS track plotting☆117Updated 2 months ago
- Estimation of Promoter Activity from RNA-Seq data☆56Updated 5 months ago
- Analysis of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in cancer☆98Updated 4 years ago
- A toolset for profiling alternative splicing events in RNA-Seq data.☆83Updated 11 months ago
- toolbox for analysing BS-seq data, advance features in SNV, ASM and DMR☆67Updated 2 years ago
- An R package to Identify, Annoatate and Visialize Isoform Switches with Functional Consequences (from RNA-seq data)☆120Updated last month
- ☆32Updated 7 years ago
- Fast, integrative fine mapping with functional data☆61Updated 6 years ago
- Scripts to import your FeatureCounts output into DEXSeq☆34Updated 7 years ago
- A quickstart tool for AmpliconArchitect. Enables all steps (alignment, CNV calling, seed interval detection) prior to running AmpliconArc…☆76Updated last week
- This is the Gviz development repository. Gviz plots data and annotation information along genomic coordinates.☆88Updated 11 months ago
- Workflows for processing RNA data for germline short variant discovery with GATK v4 and related tools☆83Updated 4 years ago
- Allele-specific alignment sorting☆61Updated 2 years ago