User: craigdj91

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craigdj910
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Filtering out incorrect index combinations in fastq file
... I have a combined paired-end FASTQ file where each sequence begins with a 14 bp unique index, allowing me to group reads together that come from the same original template molecule--very similar concept to sample barcoding where reads are grouped together based on what sample they belong to; however ...
sequencing next-gen perl software error written 6 days ago by craigdj910

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