Hello, I'm performing RNAseq analyses and I've stumbled upon some puzzling results.
I aligned some data with tophat2 (default settings) and as long as the results were disappointing (only about 5% of properly paired reads) I changed the -r and --mate-std-dev parameters and gotten to 60% (I know, still not very high). I ran htseq_count on the resulting bam alignments and comparing the two results I see no differences.
Am I missing something? Does htseq_count use the information about properly paired reads or not? By these results I am prone to say no, I will check the code...
I aligned some data with tophat2 (default settings) and as long as the results were disappointing (only about 5% of properly paired reads) I changed the -r and --mate-std-dev parameters and gotten to 60% (I know, still not very high). I ran htseq_count on the resulting bam alignments and comparing the two results I see no differences.
Am I missing something? Does htseq_count use the information about properly paired reads or not? By these results I am prone to say no, I will check the code...
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