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multithreading smalt error #71
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Could you share the input reads with me please so I can try to debug? Thanks. |
Hi,
Here they are! They have already been trimmed with trimmomatic. Thanks so
much.
Best,
fastqs.zip
<https://drive.google.com/file/d/0B0s7NWreQ5QqWUpNcnFxcVB4LVE/view?usp=drive_web>
Louise
…On Tue, Feb 14, 2017 at 5:14 AM, martinghunt ***@***.***> wrote:
Could you share the input reads with me please so I can try to debug?
Thanks.
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Thanks. What version of IVA did you use and what was the command to run it? |
IVA version 1.0.8
Using kmc version 2.1.1
Using kmc_dump version 2.1.1
Using nucmer version 3.1
Using samtools version 1.3.1
Using smalt version 0.7.6
iva -f 6390_S23_L001_R1_001.trimmed.fastq -r
6390_S23_L001_R2_001.trimmed.fastq IVA_output
…On Tue, Feb 14, 2017 at 10:12 AM, martinghunt ***@***.***> wrote:
Thanks. What version of IVA did you use and what was the command to run it?
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I don't yet know why you didn't get the error with a single thread, but the reason for the error is that there needs to be the same number of reads in the two files. And the N^th read in each file should be mate pairs.
If you trim with trimmomatic, then you'll need to only keep the paired reads. Throw away everything else, ie when one read of a pair is removed by trimmomatic. |
Thank you, I will try that. I assume that it is not possible to run IVA on
unpaired reads?
…On Tue, Feb 14, 2017 at 10:40 AM, martinghunt ***@***.***> wrote:
I don't yet know why you didn't get the error with a single thread, but
the reason for the error is that there needs to be the same number of reads
in the two files. And the N^th read in each file should be mate pairs.
$ wc -l *
1989088 6390_S23_L001_R1_001.trimmed.fastq
1657760 6390_S23_L001_R2_001.trimmed.fastq
If you trim with trimmomatic, then you'll need to only keep the paired
reads. Throw away everything else, ie when one read of a pair is removed by
trimmomatic.
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No, sorry but the read pair information is essential to its algorithm. |
I see, I thought so. Thanks for the very quick reply, I really appreciate
it!
…On Tue, Feb 14, 2017 at 10:44 AM, martinghunt ***@***.***> wrote:
No, sorry but the read pair information is essential to its algorithm.
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When running IVA on full genome influenza samples and enabling multiple threads, I get the following smalt error:
smalt.c:807 ERROR: The two FASTA/FASTQ input file have different numbers of reads
[W::sam_read1] parse error at line 812880
[main_samview] truncated file.
I do not get this error if I run the same sample with a single thread.
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