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I would like to know how deconvulation of sequence files is being done.
Would appreciate if someone could guide me to a resource or process.
Supplementary note 2 mentions about it very briefly, would like a little more context.
Jonathan Schmid-Burgk
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May 18, 2020, 5:47:58 PM5/18/20
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Hi Dan,
The deconvolution is currently implemented in most simple fashion, just count reads with perfect viral genome match, then increment a counter for the adjacent barcode, finally output a list of barcodes with their read numbers. I write all code in javascript as it's ok fast and runs on nearly every device
Best,
Jonathan
David Li
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Jun 11, 2020, 12:15:27 AM6/11/20
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