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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
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Location: Europe Join Date: Feb 2013
Posts: 58
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Hi,
I have technical replicate fastq files for some samples. For an example I have technical replicates like control_1a.fastq and control_1b.fastq. I would like to combine these two replicates as a single fastq file and do the same thing for other replicates also. is the following way of doing is right? cat control_1a.fastq control_1b.fastq > Control_1.fastq Kindly guide me. |
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#2 |
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Location: East Coast USA Join Date: Feb 2008
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If source files are not compressed then that should be fine.
Edit: If files are compressed then see the caveat in post #4. Last edited by GenoMax; 03-27-2015 at 07:22 AM. Reason: added a caveat |
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#3 |
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Location: Europe Join Date: Feb 2013
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#4 | |
Senior Member
Location: East Coast USA Join Date: Feb 2008
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Example below is from a recent presentation by Drs. Simon Andrews and Tim Stevens (Babraham Institute, UK).
----------------------------------- If you have gzipped fastq files then are the following result files equivalent? Code:
$ cat seq1.fq.gz seq2.fq.gz > all1.fq.gz $ zcat seq1.fq.gz seq2.fq.gz | gzip -c > all2.fq.gz Explanation: Quote:
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Tags |
concatenation, fastq, technical replicates |
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