nf-core / dualrnaseqLinks
Analysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.
☆24Updated 3 months ago
Alternatives and similar repositories for dualrnaseq
Users that are interested in dualrnaseq are comparing it to the libraries listed below
Sorting:
- ☆23Updated 8 months ago
- ☆23Updated 4 years ago
- Benchmarking of aligners and variant callers for Whole Exome Sequencing data☆20Updated 6 years ago
- visual analysis of your VCF files☆36Updated 2 years ago
- ☆12Updated 3 years ago
- a set of NGS pipelines☆24Updated 2 weeks ago
- A Nextflow Genome-Wide Association Study (GWAS) Pipeline☆35Updated 3 months ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 3 years ago
- UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets☆34Updated 6 months ago
- Geared towards life scientists wanting to be able to understand and use basic statistical and machine learning methods☆16Updated 3 months ago
- Tool for RNA-Seq analysis.☆39Updated 3 years ago
- A networks analysis pipeline for RNASeq time series data☆14Updated 4 years ago
- A Python3-base pipeline for translated circular RNA(circRNA) identification☆17Updated this week
- scripts for RNA-Seq analysis☆28Updated 3 years ago
- pathway based data integration and visualization☆41Updated 6 months ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆36Updated last year
- Gene Set Enrichment Analysis and Over Representation Analysis analysis using R☆20Updated 6 years ago
- tspex: tissue-specificity calculator☆33Updated 2 years ago
- Merge fastq files split over lanes☆20Updated 7 years ago
- RNA-seq workflow for Snakemake based on STAR and featureCounts.☆23Updated 6 years ago
- Accurate estimation and robust modelling of translation dynamics at codon resolution☆20Updated 8 years ago
- An efficient way to guess the library type of your RNA-Seq data.☆32Updated 2 years ago
- Provides Quality Control of sequencing samples by deducing if there is batch effect and adjusts for it.☆35Updated 2 years ago
- Documentation for vcfR☆11Updated 4 months ago
- Rapid analysis and visualisation for bulk RNA-seq, psuedo-bulk RNA-seq, GeoMx and Proteomic datasets.☆30Updated last year
- The Zavolab Automated RNA-seq Pipeline☆35Updated 2 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 6 months ago
- A pipeline for differential expression and differential alternative splicing analysis☆66Updated last year
- Evolutionary Transcriptomics with R☆45Updated this week
- A command line tool to compute mapping statistics from a BAM file☆24Updated 3 years ago