Hello,
Hopefully there is a simple way to do this that I am unaware of.
I have fastq and bam files (100bp paired end Illumina). In the alignment files there are lots of areas with one or a few reads spread throughout the genome.
What I would like to do is either sort results to visualize, for example in Integrative Genomics Viewer, or generate a list that will show in descending order the locations that have the greatest number of reads or the greatest coverage. This would most likely be within a window, say 50bp.
For example:
chr21:33,031,597 has 58 reads
chr21:33,031,200 has 56 reads
chr21:33,025,000 has 42 reads
and so on.
Any advice or guidance on different ways I might achieve this is very appreciated.
Thank you
Hopefully there is a simple way to do this that I am unaware of.
I have fastq and bam files (100bp paired end Illumina). In the alignment files there are lots of areas with one or a few reads spread throughout the genome.
What I would like to do is either sort results to visualize, for example in Integrative Genomics Viewer, or generate a list that will show in descending order the locations that have the greatest number of reads or the greatest coverage. This would most likely be within a window, say 50bp.
For example:
chr21:33,031,597 has 58 reads
chr21:33,031,200 has 56 reads
chr21:33,025,000 has 42 reads
and so on.
Any advice or guidance on different ways I might achieve this is very appreciated.
Thank you
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