User: drthippeshhs

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Considerations for trimming poor quality Illumina MiSeq paired end reads
... I have generated fastq files from Illumina MiSeq for bacterial genome sequencing. My reads are 2 X 300 bp paired end reads. I checked quality of the reads in FastQC and found that Q score goes below 26 for forward reads from base position 200 and Q score goes below 26 from base position 135 in reve ...
fastq alignment assembly qa written 11 months ago by drthippeshhs0 • updated 11 months ago by Jennifer Hillman Jackson25k

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