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Trimmomatic fails for sequencing data generated by the Element Biosciences AVITI instrument if Phred33/64 encoding is not provided (quality score is autodetected for Illumina data).
"Error: Unable to detect quality encoding"
Adding the "-phred33" argument solves the issue.
The text was updated successfully, but these errors were encountered:
Unfortunately it's not always possible to tell the quality offset of a FASTQ file, since the symbols used overlap. Trimmomatic relies on finding some quality symbols (within the early part of the file) which are informative - a low quality base in PHRED-33 (which would imply a negative quality score in PHRED-64) or a high quality base in Phred-64 (which would give a quality score >40 in PHRED-33).
A FASTQ file encoded PHRED-33 with quality scores from 31-40 looks the same as a PHRED-64 encoding with quality scores 0-9. I guess your file falls into this category (at least in the first chunk)
Trimmomatic fails for sequencing data generated by the Element Biosciences AVITI instrument if Phred33/64 encoding is not provided (quality score is autodetected for Illumina data).
"Error: Unable to detect quality encoding"
Adding the "-phred33" argument solves the issue.
The text was updated successfully, but these errors were encountered: