Hi, guys,
I'm sorry, I make a mistake, there is no problem, but I don't know how to delete the problem.
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I faced a problem when mapping again...
I used Bowtie to align CLIP-seq reads to genome with the parameter "-v 1" which allow the reads have one mismatch. But in the result, Bowtie treat all the nucleotides of reads as insertion. For example:
2-42 16 chr11 86397621 255 23M * 0 0 GTCAACATCAGTCTGATAAGCTA IIIIIIIIIIIIIIIIIIIIIII XA:i:0 MD:Z:23 NM:i:0
Does any one have any idea what happened? What should I do to make it work?
Thanks,
Yue
I'm sorry, I make a mistake, there is no problem, but I don't know how to delete the problem.
-------------------------------------------------------------------------------------------------------
I faced a problem when mapping again...
I used Bowtie to align CLIP-seq reads to genome with the parameter "-v 1" which allow the reads have one mismatch. But in the result, Bowtie treat all the nucleotides of reads as insertion. For example:
2-42 16 chr11 86397621 255 23M * 0 0 GTCAACATCAGTCTGATAAGCTA IIIIIIIIIIIIIIIIIIIIIII XA:i:0 MD:Z:23 NM:i:0
Does any one have any idea what happened? What should I do to make it work?
Thanks,
Yue
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