Question: Question About Fastq Groomer
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gravatar for Timothy Hughes
8.6 years ago by
Timothy Hughes20 wrote:
Hi Jianchao, The different fastq formats are broadly summarised by: S - Sanger Phred+33, 41 values (0, 40) I - Illumina 1.3 Phred+64, 41 values (0, 40) X - Solexa Solexa+64, 68 values (-5, 62) However, at least in my version of the MAQ software (some months old), sol2sanger conversion converts from X to S and NOT from I to X. So if you feed I to the MAQ converter you are going to get slightly incorrect Sanger qualities (because it is expecting the input qualities to have been calculated using the Solexa formula but they have in fact been calculated using Phred). If you search on seqanswers.com you will find a post that details how you need to modify the MAQ conversion script to make the conversion from I to S. Could this explain the discrepancies you observe? Tim. -- Tim Hughes PhD (http://digitised.info) Medical Genetics Department Oslo University Hospital Ullevĺl Kirkeveien 166 0407 Oslo Norway
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ADD COMMENTlink modified 8.6 years ago • written 8.6 years ago by Timothy Hughes20
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gravatar for Timothy Hughes
8.6 years ago by
Timothy Hughes20 wrote:
Here is a link to the post showing you how to modify the maq script to enable it for Illumina to Sanger conversion. http://seqanswers.com/forums/showthread.php?t=1453&highlight=conversio n+solexa+illumina+sanger Tim. -- Tim Hughes PhD (http://digitised.info) Medical Genetics Department Oslo University Hospital Ullevĺl Kirkeveien 166 0407 Oslo Norway
ADD COMMENTlink written 8.6 years ago by Timothy Hughes20
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