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shengweima — Thu, 16 Feb 2017 09:40:16 -0000

the second order is:clumpify.sh in=M27454_1_clean.fq.gz in2=M27454_2_clean.fq.gz out=M27454_1_reorder.fq.gz out2=M27454_2_reorder.fq.gz reorder

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shengweima — Thu, 16 Feb 2017 09:33:27 -0000

Dear Brian,
I have a big DNA_seq file (fastq.gz) and I want to denovo assembly, but the computer resource isn't enough. I want to remove duplicates and reorder by Clumpify, then split the one big file to many small files that the computer can do it. can you give me some suggestion?
The below is the order I used:
1. clumpify.sh in=M27454_1.fq.gz in2=M27454_2.fq.gz out=M27454_1_clean.fq.gz out2=M27454_2_clean.fq.gz dedupe subs=0
2. clumpify.sh in=M27454_1_clean.fq.gz in2=M27454_2_clean.fq.gz out=M27454_1_reorder.fq.gz out2=M27454_2_reorder.fq.gz
3. zcat M27454_1_reorder.fastq.gz | split -l 10000000 --additional-suffix=".fastq" --filter='gzip > $FILE.gz' - "XXX_"

Home modified by Brian Bushnell

Brian Bushnell — Wed, 19 Feb 2014 19:29:57 -0000

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