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Thread | Thread Starter | Forum | Replies | Last Post |
Threshold quality score to determine the quality read of ILLUMINA reads problem | edge | Illumina/Solexa | 35 | 11-02-2015 11:31 AM |
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#1 |
Junior Member
Location: orlando Join Date: Feb 2019
Posts: 1
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Hello all!
I'm new to the community and just started my first bioinformatics project. I'm filtering out merged reads with the expected error of 1-100. code I'm running: vsearch -fastq_filter ./MergedFiles/${otp}_merged.fastq -fastq_maxee 1 -fastqout ./MergedFiles/${otp}_mergedfilt.fastq -fastaout ./MergedFiles/${otp}_mergedfilt.fasta The issue is that when I run it, I get back a fatal error saying- Reading input file 0% Fatal error: FASTQ quality value (42) above qmax (41) I've tried usearch, but my file is too big for the free 32-bit version, and I've tried replacing fastq_maxee 1 with fastq_qmax 42, but that doesn't filter anything out. I'm a bit new to all this and I'm stuck. Any help would be greatly appreciated! -science panda |
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Tags |
fastq, fastq quality, fastq quality numbers, vsearch |
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