User: mtp1v12

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mtp1v120
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Posts by mtp1v12

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Comment: C: Making paired-end reads the same length
... Thank you for the reply Jennifer.  I'm using Bowtie2 to map.  The data is Illumina.  I think I have the raw reads (sent from collaborator in Japan).  I have used FASTQ groomer only, i'm not aware of any other manipulation.  Thank you for your help. ...
written 2.8 years ago by mtp1v120
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Making paired-end reads the same length
... I have paired-end data (in two separate files).  I have groomed my files, and would like to filter the reads for quality.  However, the read lengths for some of the paired reads are not equal.  If I filter the files independently, the mapping fails as the two files contain different numbers of reads ...
filter galaxy bowtie fastq written 2.8 years ago by mtp1v120

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