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Subread

Table of Contents

Introduction

Subread package: high-performance read alignment, quantification and mutation discovery

The Subread package comprises a suite of software programs for processing next-gen sequencing read data including:

 

Subread: a general-purpose read aligner which can align both genomic DNA-seq and RNA-seq reads. It can also be used to discover genomic mutations including short indels and structural variants.

Subjunc: a read aligner developed for aligning RNA-seq reads and for the detection of exon-exon junctions. Gene fusion events can be detected as well.

featureCounts: a software program developed for counting reads to genomic features such as genes, exons, promoters and genomic bins.

exactSNP: a SNP caller that discovers SNPs by testing signals against local background noises.

These programs were also implemented in Bioconductor R package Rsubread.

Restrictions / License Information

GNU GENERAL PUBLIC LICENSE

Running Instructions

 

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Version 1.5.2