doTopHat2: Read alignment using the TopHat v2 aligner

Description Usage Arguments Value Author(s) References See Also

Description

Read alignment using the TopHat v2 aligner based on [1].

Usage

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  doTopHat2(...)
  ## S3 method for class 'FastqDataSet'
doTopHat2(dataSet, reference, transcripts, ..., verbose=FALSE)

Arguments

dataSet, df

A FastqDataSet.

reference

A FastaReferenceFile or a Bowtie2IndexSet specifying the genome reference to align the FASTQ reads to.

transcripts

A GtfDataFile or NULL specifying known transcripts and/or gene model annotations.

...

Additional arguments passed to TopHat2Alignment.

verbose

See Verbose.

Value

Returns a BamDataSet.

Author(s)

Henrik Bengtsson

References

[1] TopHat - A spliced read mapper for RNA-Seq, 2015. http://ccb.jhu.edu/software/tophat/
[2] Trapnell et al. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat Protoc, 2012.

See Also

For more details, see TopHat2Alignment.


HenrikBengtsson/aroma.seq documentation built on Feb. 15, 2021, 2:21 a.m.