Hi,
While I use tophat to align rnaseq, if my data is strand-specific, do I need to add the option --library-type?
What is the default settings in tophat for that.
thanks,
Ch
Hi,
While I use tophat to align rnaseq, if my data is strand-specific, do I need to add the option --library-type?
What is the default settings in tophat for that.
thanks,
Ch
yes library-type. Then you need to know the way the library was prepared. Currently the dUTP protocol is mostly used and for this you need to specify --library-type fr-firststrand. Default is fr-unstranded.
The reads will be always map to the same locations irrespective of correctness of library-type (not tested). Downstream analysis will be affected: cufflinks and htseq count when the data is in the wrong orientation or no orientation is given.
Map 1. with unstranded and then you see the result (i.e. if the data is really stranded in a genome browser).
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What do you mean by strand specific?
The library was prepared by strand-specific assay