Hi,
I ran TopHat on my RNA-Seq data and I am trying to get a sense of the total number of reads that aligned to anywhere in my reference sequence. Does the accepted_hits.sam file that is part of the TopHat output also report the alignments from the de novo junction discovery? In other words, in order to obtain the total number of mapped reads, can I just use the alignment statistics from the SAM file, or do I also need to add to that the junction counts from the junctions.bed file (5th column reporting the number of alignments spanning each junction)?
Thanks.
I ran TopHat on my RNA-Seq data and I am trying to get a sense of the total number of reads that aligned to anywhere in my reference sequence. Does the accepted_hits.sam file that is part of the TopHat output also report the alignments from the de novo junction discovery? In other words, in order to obtain the total number of mapped reads, can I just use the alignment statistics from the SAM file, or do I also need to add to that the junction counts from the junctions.bed file (5th column reporting the number of alignments spanning each junction)?
Thanks.
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