Rsubread is a toolbox developed for the analyses of second and third generation sequencing data. It can be used for read mapping, read counting, SNP calling, structural variant detection and gene fusion discovery. It can be applied to all major sequencing techologies and it is suitable for the analysis of both short and long reads.
|Author||Wei Shi and Yang Liao with contributions from Gordon K Smyth, Jenny Dai and Timothy Triche, Jr.|
|Bioconductor views||Alignment ChIPSeq GeneExpression GeneRegulation GeneticVariability Genetics GenomeAnnotation Preprocessing QualityControl RNASeq SNP SequenceMatching Sequencing Software|
|Date of publication||2018-07-11|
|Maintainer||Wei Shi <[email protected]>, Yang Liao <[email protected]> and Gordon K Smyth <[email protected]>|
|Package repository||View on Bioconductor|
Install the latest version of this package by entering the following in R:
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.