Search
Question: How to build a RNA-seq table of counts for repeatmasker annotations
0
gravatar for Robert Castelo
19 days ago by
Robert Castelo2.0k
Spain/Barcelona/Universitat Pompeu Fabra
Robert Castelo2.0k wrote:

hi all,

i'm interested in building a table of counts from BAM files produced by a PE RNA-seq experiment, for RepeatMasker annotations. essentially to know how many RNA-seq reads map to a particular LTR, etc. i've searched for those annotations among the Bioconductor annotation packages but couldn't find anything with the keyword repeat. searching on the support site led me to this Rsubread::featureCounts extremely slow on some annotations on the performance of featureCounts for that purpose but it has no details about how the annotations are input to the software. i'm familiar with using 'summarizeOverlaps()' from the GenomicAlignments package to build a table of counts from gene annotations, which i find it convenient because the input is a 'TxDb' object and the output is a 'SummarizedExperiment' object. any hint about how to do this in Bioconductor will be very appreciated.

thanks!!

robert.

ADD COMMENTlink modified 19 days ago by Michael Lawrence9.8k • written 19 days ago by Robert Castelo2.0k
2
gravatar for Michael Lawrence
19 days ago by
United States
Michael Lawrence9.8k wrote:

You can always download the "rmsk" table from UCSC using rtracklayer.

ADD COMMENTlink written 19 days ago by Michael Lawrence9.8k

thanks for the tip. i've seen that section 5.1 of the vignette of rtracklayer contains an example about importing repeatmasker annotations for genomic regions. however, because i need to work with the whole set of annotations, i can't use that approach since it would take too long. i've downloaded the rmsk.txt.gz file directly from UCSC but now the question is whether this can be imported into R/BioC with rtracklayer. i've tried the 'import()' function with different formats and none seem to work. before i end up writing my own parser, is there a way to import the rmsk.txt.gz file with rtracklayer? thanx.
 

ADD REPLYlink written 19 days ago by Robert Castelo2.0k

Probably could just read it with read.table() and then coerce to GRanges.

ADD REPLYlink written 19 days ago by Michael Lawrence9.8k

True, that was it, thanks!

ADD REPLYlink written 12 days ago by Robert Castelo2.0k
Please log in to add an answer.

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.2.0
Traffic: 314 users visited in the last hour