Just wondering is it possible to group the reads by the cluster they
came from on the flowcell. We want to do so to get an idea of regions(clusters)
contributing to low/high quality reads and compare GC.
I have noticed the fastq header has the X|Y coordinates but not sure how to cluster them together to determine the boundaries of each cluster.
Thanks!
-Abhi
came from on the flowcell. We want to do so to get an idea of regions(clusters)
contributing to low/high quality reads and compare GC.
I have noticed the fastq header has the X|Y coordinates but not sure how to cluster them together to determine the boundaries of each cluster.
Thanks!
-Abhi
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