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#

featurecounts

Here are 14 public repositories matching this topic...

bioinfo-notebook

🔬 Bioinformatics Notebook. Scripts for bioinformatics pipelines, with quick start guides for programs and video demonstrations.

  • UpdatedNov 12, 2020
  • Shell

Scripts to import your FeatureCounts output into DEXSeq

  • UpdatedOct 27, 2018
  • Python

A tool for extraction of lexical features from text based on UIMA and MapReduce

  • UpdatedAug 24, 2018
  • Java

This is a code tutorial for rna or dna sequence mapping by myself-RyanYip

  • UpdatedDec 10, 2018
  • Shell

This repository contatins a pipeline for RNA-Seq data processing using featurecounts for gene count generation

  • UpdatedMar 19, 2024
  • Shell

Scripts to index and align Bovine genome with HISAT2

  • UpdatedMay 22, 2018
  • Shell

nextflow ATACseq pipeline for GG02

  • UpdatedMay 20, 2024
  • Nextflow

Build Docker container for Subread package and (optionally) convert to Apptainer/Singularity.

  • UpdatedMar 4, 2023
  • Dockerfile

A pipeline to call intron and intergenic eRNAs from PRO-seq Data

  • UpdatedFeb 19, 2024
  • Shell

Proof of concept of a RNA-Seq pipeline from reads to count matrix (including quality control) with Nextflow and additional example RNA-Seq analysis in R

  • UpdatedJan 12, 2022
  • HTML

A reproducible RNA-Seq analysis pipeline for Staphylococcus aureus under antibiotic stress, utilizing Nextflow and Singularity. It involves genome mapping, read counting, and statistical analysis to identify differentially expressed genes (DEGs) and generates key visualizations.

  • UpdatedDec 9, 2024
  • R

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