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Hello,
I extracted fastq from the duplex_orig.sam and compared output to the original raw reads.
In the following alignment file, The top sequence is the output for the duplex read. Below it are the two corresponding reads. Last read is reverse complemented.
The highlighted region shows 'A' in the duplex output while it shows 'C' in read1 and 'T' in reverse complement of read2.
My understanding is, for this locus, the duplex should show either C or T but not A.
Can you please share some insights?
Thanks
-Dev

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