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Old 07-16-2013, 02:09 AM   #1
priya
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Location: sweden

Join Date: Apr 2013
Posts: 57
Default 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?
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