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  • priya
    Member
    • Apr 2013
    • 57

    #1

    Read1 and Read2 are not consistent

    Hi, I got the sequencing data from Illumina HiSeq2000. Its pairend sequencing.
    The two fastq files(read1 and read2) does not contain equal number of lines.
    19166068 read1.fastq
    19295372 read2.fastq

    Is there any way that I can make them equal by removing the lines which are not there in read1 file?
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Yeah, have a look at this thread on Biostars for some example commands. Allegedly, you can also use cmpfastq, which is a perl script, to do this too (I've never used this so I can't say that it works properly).

    In the future, use a trimmer that handles both reads of a pair at once so you can avoid these issues.

    Comment

    • priya
      Member
      • Apr 2013
      • 57

      #3
      Originally posted by dpryan View Post
      Yeah, have a look at this thread on Biostars for some example commands. Allegedly, you can also use cmpfastq, which is a perl script, to do this too (I've never used this so I can't say that it works properly).

      In the future, use a trimmer that handles both reads of a pair at once so you can avoid these issues.
      Thanks for your reply.I will look into it..

      Comment

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