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Thread | Thread Starter | Forum | Replies | Last Post |
Difference between "bedtools bamtofastq" and Picard's SamToFastq | thedamian | Bioinformatics | 3 | 01-21-2014 06:00 AM |
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Picard SamtoFastq Extract Only Paired Reads | fongchun | Bioinformatics | 3 | 10-09-2012 12:54 AM |
Picard SamToFastq is prior sort needed? | vinay052003 | Bioinformatics | 0 | 04-25-2012 09:59 PM |
Strange contigs | Ramet | RNA Sequencing | 0 | 06-08-2011 05:53 AM |
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#1 |
Member
Location: Scotland Join Date: Feb 2014
Posts: 27
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Dear all,
I am using picard SamtoFastq in oredr to convert BAM/SAM to fastq. I have a paired end sample. I am using following command:- java -jar SamToFastq.jar INPUT=input.bam FASTQ=input_1.fastq SECOND_END_FASTQ=input_2.fastq VALIDATION_STRINGENCY=LENIENT The command runs without error and generate two file. Now the problem is input_1.fastq has all the reads where as input_2.fastq is empty(o byte file). I have no idea why it's happening. I tried following option but no luck, 1) Sorted bam -> SamToFastq 2) BAM to SAM -> SamToFastq Any suggestion would be very helpful. Thanks, Reema SIngh |
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#2 |
Senior Member
Location: Budapest Join Date: Mar 2010
Posts: 329
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Maybe you BAM file is not a paired end sample. Check it manually.
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#3 |
Member
Location: Scotland Join Date: Feb 2014
Posts: 27
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