fuxialexander / marvel
Multigranular Analysis of Regulatory Variants on the Epigenomic Landscape
☆9Updated 4 years ago
Alternatives and similar repositories for marvel
Users that are interested in marvel are comparing it to the libraries listed below
Sorting:
- R interface to genome annotation files and the UCSC genome browser☆32Updated last month
- RNA-seq data comprehensive data analysis toolbox☆19Updated 2 years ago
- Bedfile perturbation tool☆17Updated last year
- Exome/Capture/RNASeq Pipeline Implementation using snakemake☆19Updated 5 years ago
- A web-browser app to visualise, interpret and prioritise genomic/transcriptomic structural variations (SVs) of multiple samples.☆10Updated last week
- Chromatin ACcessibility and Transcriptomics Unifying Software☆16Updated 6 months ago
- Code for EpiMap data browser☆14Updated 11 months ago
- stageR package☆13Updated 2 years ago
- Converts 'MultiQC' Reports into Tidy Data Frames☆19Updated last year
- Differential expression and allelic analysis, nonparametric statistics☆29Updated 4 months ago
- Hera-T, a fast and accurate tool for estimating gene abundances in single cell data generated by the 10X-Chromium protocol☆17Updated 3 years ago
- A Snakemake pipeline for Quality Control of Whole Genome Sequencing data☆14Updated 3 years ago
- ☆16Updated 2 years ago
- ☆12Updated last year
- INTERSTELLAR: Interpretation, scalable transformation, and emulation of large-scale sequencing reads☆18Updated 11 months ago
- Lightweight Python interfaces for reading, writing, and querying Genomic Regions (BED)☆14Updated last month
- Library for visualising genomic features in Python.☆15Updated 8 years ago
- Manage Files Across Sessions☆13Updated this week
- ☆17Updated 9 months ago
- Nascent Transcription Processing Pipeline☆19Updated last week
- Artisanal 🤣 bioinformatics tools and pipelines in Scala☆20Updated 5 years ago
- Workflow for ZINB-WaVE + DESeq2 intergration for single-cell RNA-seq☆31Updated 4 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- Build an index for your BAM Index (BAI)☆17Updated 10 years ago
- ☆26Updated 2 years ago
- Cookiecutter profile for making a NextFlow-based bioinformatics tool☆16Updated 10 months ago
- Code for RNA-seq gene coexpression analysis☆9Updated 3 years ago
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆37Updated last year
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 3 years ago
- ☆12Updated last year