Kanchan
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Kanchan
Hello, I am trying to use porechop for adaptor trimming on nanopore reads. I constantly get the following error: Error: input_reads.fastq could not be parsed - is it formatted correctly?...
Hello, 1. I am running porechop on 1 D^2 data using the following command. `porechop -i input_reads.fastq.gz -o output_reads.fastq.gz` For 1D ~98% reads were trimmed for adaptors. however, for 1D^2...