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Sang Chul Choi
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230
@sang-chul-choi-5066
Last seen 10.2 years ago
Hi,
I am trying to use "qrqc" package. I had two fastQ files (Illumina),
one of which created about a year ago, and another was created a few
months ago. The earlier one was read in using readSeqFile, and the
latter one was not. I attach the error message from it with R version.
The problem is about quality score format. I tried quality="phred"
because for earlier one quality scores are Illumina Q score offset
(ascii 64), and for latter one is in Sanger FASTQ format, the offset
is ascii 33. I am wondering if I could change readSeqFile options to
read the second fastQ file that is in Sanger FASTQ format created by
Illumina.
Thank you,
SangChul
Error messages.
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> fq.file <- readSeqFile("1.fq.gz")
Error in readSeqFile("FASTQ019.fq.gz") :
base quality out of range (0 <= b <= 62) encountered: 35
> fq.file <- readSeqFile("1.fq.gz",quality="phred")
Error in readSeqFile("FASTQ019.fq.gz", :
base quality out of range (4 <= b <= 60) encountered: 61
=========================================================
R version and sessionInfo.
=========================================================
R Under development (unstable) (2012-02-14 r58341)
Copyright (C) 2012 The R Foundation for Statistical Computing
ISBN 3-900051-07-0
Platform: x86_64-apple-darwin10.8.0 (64-bit)
other attached packages:
[1] qrqc_1.3.0 ShortRead_1.13.12 latticeExtra_0.6-19
[4] RColorBrewer_1.0-5 Rsamtools_1.7.33 lattice_0.20-0
[7] Biostrings_2.23.6 GenomicRanges_1.7.24 IRanges_1.13.24
[10] BiocGenerics_0.1.4
=========================================================