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Thread | Thread Starter | Forum | Replies | Last Post |
How to demultiplex NEXTERA EXOME RAPID DATA run in a Hiseq 2500 | frossit | Illumina/Solexa | 4 | 11-26-2013 08:52 AM |
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BCL to FASTQ conversation for paired-end RNA data | seqmonkey | Illumina/Solexa | 8 | 09-27-2011 12:02 PM |
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#1 |
Senior Member
Location: Germany Join Date: May 2010
Posts: 150
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Hi,
I was wondering if anyone has experience in demultiplexing BCL files from Illumina with two different barcoding systems in one go? we would like to know whether it is possible to use different, barcoded Tn5 adaptors during tagmentation and then use those Barcodes in combination with the barcodes on the sequencing primers to demultiplex the samples. Has anyone has experience with this kind of analysis? Is it possible to only add the Tn5 sequence to the primer sequence before demultiplexing and use it in the BCL2fastq run? thanks |
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Tags |
demultiplexing, library perparation, primer, tagmentation |
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