Hello all,
I've recently tried to process few miRNA-seq experiments for our collaborators.
The library is quite duplicated but I guess that's to be expected with miRNA; you have about 10-fold duplicate rate for most I managed to look at with FastQC
I've got (what seems to be) the correct settings for STAR and got a fairly nice looking BAM, with some miRNAs (from miR-base) having thousands of reads according to the index. But both IGV and counting tools don't see most of those reads!
The mapping qualities are fairly good, all the names are unique (I've looked at the specific position in the BAM file manually), and about 6 thousand have NH field set to 1! So these are unique reads that clearly align in the specified location - and yet they are ignored by both IGV and most read counters (I've tried featureCounts with multimapper option on, and RSEM so far).
Help me out, I'm going insane here.
I've recently tried to process few miRNA-seq experiments for our collaborators.
The library is quite duplicated but I guess that's to be expected with miRNA; you have about 10-fold duplicate rate for most I managed to look at with FastQC
I've got (what seems to be) the correct settings for STAR and got a fairly nice looking BAM, with some miRNAs (from miR-base) having thousands of reads according to the index. But both IGV and counting tools don't see most of those reads!
The mapping qualities are fairly good, all the names are unique (I've looked at the specific position in the BAM file manually), and about 6 thousand have NH field set to 1! So these are unique reads that clearly align in the specified location - and yet they are ignored by both IGV and most read counters (I've tried featureCounts with multimapper option on, and RSEM so far).
Help me out, I'm going insane here.
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