shortread error?
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wang peter ★ 2.0k
@wang-peter-4647
Last seen 10.2 years ago
i am running a pipeline to clean the reads there was an error Error in add(raw()) : record does not start with '@' Calls: trimRead -> yield -> yield -> <anonymous> -> add -> .Call Execution halted i never met it before,i think that is maybe due to data problem? one fastq record start without '@' -- shan gao Room 231(Dr.Fei lab) Boyce Thompson Institute for Plant Research Cornell University Tower Road, Ithaca, NY 14853-1801 Office phone: 1-607-254-1267(day) Official email:sg839 at cornell.edu Facebook:http://www.facebook.com/profile.php?id=100001986532253
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@martin-morgan-1513
Last seen 4 months ago
United States
On 01/23/2013 07:55 PM, Wang Peter wrote: > i am running a pipeline to clean the reads > > there was an error > Error in add(raw()) : record does not start with '@' > Calls: trimRead -> yield -> yield -> <anonymous> -> add -> .Call > Execution halted > > i never met it before,i think that is maybe due to data problem? > one fastq record start without '@' maybe sequence and quality length mismatch, or maybe a programming error on my part. I guess you have a FastqStreamer() or FastqSampler, and you can print the streamer after the error to find out about where in the file the error is occurring. To illustrate after example(FastqStreamer) we get a file 'fl' that is a fastq file, and create a streamer > strm = FastqStreamer(fl, 100) and yield twice > yield(strm) class: ShortReadQ length: 100 reads; width: 36 cycles > yield(strm) class: ShortReadQ length: 100 reads; width: 36 cycles and then find that the current buffer holds 100 records, and we've already added 200. > strm class: FastqStreamer file: s_1_sequence.txt status: n=100 current=100 added=200 total=200 You could print out your streamer after the error to find the approximate place in the file where the error occurs. Also if it is a programming error on my part, then you can perhaps work around this by choosing a different yield size or 'readerBlockSize'; making these prime numbers might be particularly effective at avoiding the error (but I'd rather fix the bug). It would help to have more code to see what you are doing. If it is not clear that there is an error in the fastq file, then it would help to make a reproducible example (simple code and sample data file) available to me. Martin > -- Computational Biology / Fred Hutchinson Cancer Research Center 1100 Fairview Ave. N. PO Box 19024 Seattle, WA 98109 Location: Arnold Building M1 B861 Phone: (206) 667-2793
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thank u very much
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