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Merge 4 Fastq Files

Hello,

I know there have been many questions regarding merging fastq files. But I am not getting relevant answers in my situation.

I have 4 paired-ended fastq files.

s_6_1.fastq s_6_2.fastq

s_7_1.fastq s_7_2.fastq

Can I just cat the first two files and the last two files to make s_6.fastq and s_7.fastq? I would like to use these fastq files for mapping with BWA or Bowtie.

Hope to get some suggestions regarding this. Thanks, AShwin

merge fastq genome
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updated by KCC KCC • written by bashwin.u • bashwin.u

Why do you want to do that? bwa and bowtie both supports pair-end input and there doesn't really seems like the fastq are required to be merged before alignment

• 219 views • link
written by Sam Sam

yes, you can merge the _1.fastq files into one files and the _2.fastq files into another. just maintain the order (pairing) between them.

• 0 views • link
written by brentp brentp

2 answers

Try this. Mostly default settings. Where I say "-t 4" I am assuming you have 4 processors. You can drop this number if that's not the case for you.

bwa index -p mygenome -a bwtsw mygenome.fa

bwa aln -t 4 bwtsw mygenome s_6_1.fastq > s_6_1.sai
bwa aln -t 4 bwtsw mygenome s_6_2.fastq > s_6_2.sai

bwa sampe mygenome s_6_1.sai s_6_2.sai s_6_1.fastq s_6_2.fastq > s_6.sam

Merging seems unnecessarily complicated in this case. I don't know if bwa can handle that.

• 0 views • link
written by KCC KCC

If you would like to merge the files, in your case...the merging should be..

Sample1_r1 + Sample2_r1 = Sample_r1.fastq && Sample1_r2 + Sample2_r2 = Sample_r2.fastq

Then align using bowtie2.

bowtie2 -x Genome_Index -1 Sample_r1.fastq -2 Sample_r2.fastq -S out.sam

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written by GouthamAtla GouthamAtla

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