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Thread | Thread Starter | Forum | Replies | Last Post |
For MAQ: Is there a Tool to convert sanger-format fastq file to illumina-fotmat fastq | byb121 | Bioinformatics | 6 | 12-20-2013 02:26 AM |
i converted illumina fastq into sanger fastq, need advice | Aicen | Bioinformatics | 5 | 08-27-2012 07:24 AM |
Convert illumina v1.5 fastq to sanger fastq | zouzou | Bioinformatics | 29 | 05-14-2012 10:07 PM |
how to transfer sanger fastQ into illumina FastQ | sunsnow86 | Bioinformatics | 3 | 06-17-2011 03:21 PM |
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#1 |
Member
Location: Missouri Join Date: Apr 2010
Posts: 39
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Hi,
Great forum! My first post: I have Illumina 1.3+ FASTQ files that I am converting to Sanger FASTQ using maq as follows: maq sol2sanger s_1_sequence.txt s_1_sequence.fastq It runs fine, but after the conversion is done, the file size has been reduced from 4.6 GB (4615468 bytes) to 3.5 GB (3556236 bytes). Is this simply due to the change in the Phred quality score ASCII character length for each read in the file? I just wanted to make sure I wasn't losing actual sequence data. Thanks very much in advance, jjw |
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#2 |
Senior Member
Location: Phoenix, AZ Join Date: Mar 2010
Posts: 279
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The read ID information is no longer duplicated for both the read and quality information such as
My Read1 AGTC My Read1 #$%@^ Becomes My Read1 AGTC #$%@^ |
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#3 |
Member
Location: Missouri Join Date: Apr 2010
Posts: 39
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Thanks very much.
jjw |
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