Hello all.
I am using Mosaik to align an Illumina read dataset to a reference genome. The total DNA used in Illumina sequencing included DNA from more than one organism, so I would like to try a Velvet de novo assembly with the unaligned reads that Mosaik dumped into a fastq file. Our read data is paired end, which should help our de novo assembly, but Mosaik doesn't retain the paired end information when dumping reads to the fastq file.
Does anyone have a script for reorganizing a fastq file into a Velvet-acceptable order? (i.e., Read 1 from a pair is followed by Read 2, then Read 1 and Read 2 from another pair, etc.)
Thank you,
Laura Williams
I am using Mosaik to align an Illumina read dataset to a reference genome. The total DNA used in Illumina sequencing included DNA from more than one organism, so I would like to try a Velvet de novo assembly with the unaligned reads that Mosaik dumped into a fastq file. Our read data is paired end, which should help our de novo assembly, but Mosaik doesn't retain the paired end information when dumping reads to the fastq file.
Does anyone have a script for reorganizing a fastq file into a Velvet-acceptable order? (i.e., Read 1 from a pair is followed by Read 2, then Read 1 and Read 2 from another pair, etc.)
Thank you,
Laura Williams
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