dongxuemin666 / RNA-combineLinks
RNA-seq data comprehensive data analysis toolbox
☆19Updated 2 years ago
Alternatives and similar repositories for RNA-combine
Users that are interested in RNA-combine are comparing it to the libraries listed below
Sorting:
- Chromatin ACcessibility and Transcriptomics Unifying Software☆16Updated 7 months ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 3 years ago
- interactive plots for differential expression analysis☆32Updated 2 months ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 3 months ago
- Differential ATAC-seq toolkit☆27Updated last year
- DriverPower☆26Updated 4 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Interactive eQTL visualizations☆13Updated 2 years ago
- DRAGEN Tumor/Normal workflow post-processing☆22Updated last year
- a set of NGS pipelines☆24Updated last week
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆37Updated last year
- Bulk RNA-seq Data Processing, Quality Control, and Downstream Analysis Pipeline☆21Updated 5 months ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago
- 📊 An R package of RNA-seq workflow☆16Updated 3 years ago
- Comprehensive Human Expressed SequenceS☆17Updated 10 months ago
- TIMEOR: Trajectory Inference and Mechanism Exploration with Omics Data in R☆16Updated 3 years ago
- Nascent Transcription Processing Pipeline☆19Updated last week
- WES HLA Typing based on multiple alternative tools☆16Updated 4 years ago
- Create a cromphensive report of DEG list coming from any analysis of RNAseq data☆26Updated last year
- Bedfile perturbation tool☆17Updated last year
- Accurate estimation and robust modelling of translation dynamics at codon resolution☆20Updated 7 years ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Updated last year
- ☆28Updated 5 months ago
- Workflow for Sequenza, cellularity and ploidy☆18Updated last week
- Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.☆28Updated 4 years ago
- scpca-nf is the Nextflow workflow for processing Single-cell Pediatric Cancer Atlas Portal data☆13Updated last week
- BANDITS: Bayesian ANalysis of DIfferenTial Splicing☆17Updated last year
- 🧬 🦀 A fast and efficient tool to perform a genome wide Single cell Chromatin State Analysis using multimodal histone modification data.…☆28Updated 3 years ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated 2 months ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago