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#1 |
Member
Location: Oklahoma Join Date: Jan 2012
Posts: 35
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Hi all,
I have illumina genome reads for an E. coli a collaborator is studying. The prep used had a plasmid as well. I have two questions: 1) For the reads that match both (e.g. lacI gene), how can I tell which came from the plasmid and which came from the genome? 2) Should I normalize by dividing on the total reads per library or only the mapped reads in a library? Thanks in advance... Last edited by fznajar; 01-09-2019 at 01:44 PM. |
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,088
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#1 = Unless there is/are SNP's which are captured by that particular read you would not be able to tell where the read came from. I assume the sequence of the gene is otherwise identical?
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#3 |
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Location: Oklahoma Join Date: Jan 2012
Posts: 35
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You are correct GenoMax. They are identical. Appreciate it.
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#4 | |
Senior Member
Location: Québec, Canada Join Date: Jul 2008
Posts: 260
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If you'are using "bwa sampe" for aligning, the documentation says:
Quote:
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