Description Usage Arguments Value Author(s) References See Also Examples
This function process a TranscriptDb-class object disjoining overlapping genomic regions and adding additional information needed for design matrices building and fitting.
1 |
txdb |
An object of class TranscriptDb. |
disjoin |
Logical. Create disjoint exons ranges |
with.junctions |
Logical. Add 'biological junctions' |
probelen |
Reads length |
ignore.strand |
Logical. Ignore strand information |
junction.overlap |
Minimum overlap of a read with either exons for a junction read in order to be counted |
exclude.non.std |
Logical. Shall the 'non standard' chromosomes be removed? |
exclude.mir |
Logical. Remove microRNAs |
what |
What kind of exons to take into account. General "exons" or "cds" |
mcpar |
An object of (virtual) class "BiocParallelParam"
specifying parameters for parallel computing using |
verbose |
Logical. Print information during computation |
test.genes |
Character vector. Subset of gene names to consider. Basically for debugging. |
A GRangesList containing GRanges for each gene
Stefano Calza <stefano.calza@unibs.it>, Chen Suo, Agus Salim and Yudi Pawitan
Suo C, Calza S, Salim A, Pawitan Y. Joint estimation of isoform expression and isoform-specific read distribution using multisample RNA-Seq data. Bioinformatics. 2014 Feb 15;30(4):506-13
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 | ## Not run:
seqs <- seqnames(seqinfo(TxDb.Hsapiens.UCSC.hg19.knownGene))
sel <- rep(FALSE,length(seqs))
names(sel) <- seqs
sel["chr14"] <- TRUE
isActiveSeq(TxDb.Hsapiens.UCSC.hg19.knownGene) <- sel
library(TxDb.Hsapiens.UCSC.hg19.knownGene)
param = SerialParam()
txdb <- reshapeTxDb(TxDb.Hsapiens.UCSC.hg19.knownGene,probelen = 50L,mcpar=param)
## End(Not run)
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