Entering edit mode
7.6 years ago
Manuel Mendoza
▴
10
Hello,
I am working with fastq file from cDNA. A complete transcriptome was sequenced using Illumina Tech. I want to know the q-index for each read (nucleotide per nucleotide), now I am using ShortRead package (I work with R).
Does anyone know how to do it?
By "q-index (nucleotide per nucleotide)" , do you mean the average sequencing quality per base position, as discussed here?
No, I want the value of q-index per base position for each read... Something like that:
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