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Thread | Thread Starter | Forum | Replies | Last Post |
Paired-end Illumina RNA-seq adapter trimming | fabrice | Bioinformatics | 8 | 01-05-2015 08:48 AM |
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#1 |
Member
Location: EU Join Date: Sep 2010
Posts: 52
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hi
i have miseq reads of 150 * 2 paired end library. I wanted this to make it look like hiseq library 100bases. is there a way where i can keep only 100 bases in each read and trim the rest at the end to make it a 100 * 2 library? Thank you |
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#2 |
Senior Member
Location: Kansas City Join Date: Mar 2008
Posts: 197
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#3 |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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#4 | |
--Site Admin--
Location: SF Bay Area, CA, USA Join Date: Oct 2007
Posts: 1,358
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#5 |
Member
Location: hd.de Join Date: Jun 2010
Posts: 81
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or just use awk:
awk {print substr($1, 1, 100)} reads.fastq if the ID is line is longer than your desired read length: awk '{if(NR%4==1){print $1} else{print substr($1, 1, 20)}}' reads.fastq |
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#6 |
Senior Member
Location: berlin Join Date: Feb 2010
Posts: 156
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Blatant plug: Trimmomatic, you know it makes sense
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