Hello,
I am doing a comparison of duplicated reads on Illumina NovaSeq vs MGI G400 by checking the distribution of reads on the flowcell. I noticed the fastq header from the G400 is quite different from that of the NovaSeq.
For example, one of the headers is:
which I interpret as "flowcell id: F350009384", "lane: L1", "tile column: C001", "tile row: R001", "read: /1" and the remaining part "0008170" is unclear to me. Could this be the X and Y coordinates of the cluster/DNB?
Would love to hear if my interpretation is correct. Thanks!
I am doing a comparison of duplicated reads on Illumina NovaSeq vs MGI G400 by checking the distribution of reads on the flowcell. I noticed the fastq header from the G400 is quite different from that of the NovaSeq.
For example, one of the headers is:
@F350009384L1C001R0010008170/1
Would love to hear if my interpretation is correct. Thanks!
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