Hi,
I have 4 runs (4 fastq) raw data files for one sample. I would like to align the data, but wondering
1)can I concatate the 4 files into one file and then use the single file as Input to aligner tool(STAR, or Bowtie) or
2) Should I run aligment seperately on 4 fastq files and then use samtools to merge 4 bam files into single file.
which is the correct procedure to do..please guide me..
Thank you!
I have 4 runs (4 fastq) raw data files for one sample. I would like to align the data, but wondering
1)can I concatate the 4 files into one file and then use the single file as Input to aligner tool(STAR, or Bowtie) or
2) Should I run aligment seperately on 4 fastq files and then use samtools to merge 4 bam files into single file.
which is the correct procedure to do..please guide me..
Thank you!
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