Hello,
if i create fastq files from .sra files using fastq-dump (default options), what quality is used in the fastq files and which options do i need to use with bowtie mapper? (default, --solexa-quals, etc.)?
Tnx, Gregor
Hello,
if i create fastq files from .sra files using fastq-dump (default options), what quality is used in the fastq files and which options do i need to use with bowtie mapper? (default, --solexa-quals, etc.)?
Tnx, Gregor
Instead of downloading from SRA, use the same ID, search and download from EBI ENA archive in gziped fastq format, also using Aspera.
Compare:
http://www.ebi.ac.uk/ena/data/view/SRS074453
http://www.ncbi.nlm.nih.gov/sra?term=SRS074453
Reads are in phred quality scale.
There is no requirement for specific quality type for submission to SRA. So files downloaded from SRA can have any of the possible quality score scales.
[?]Here[?] is a seqanswers thread on it. You can use fastqc to check the quality score type, or try using that perl script in the thread.
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