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Getting memory error while using hg19 as reference and targeted bed file for whole exome #61
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Greetings, |
Hi Zach,
Thank you for your prompt reply 😊
I am running 1 job at a time. RAM is 16GB. No other applications are running.
Regards
Mrinal
From: zstephens <[email protected]>
Sent: Thursday, May 23, 2019 1:42 AM
To: zstephens/neat-genreads <[email protected]>
Cc: Mrinal Puranik <[email protected]>; Author <[email protected]>
Subject: Re: [zstephens/neat-genreads] Getting memory error while using hg19 as reference and targeted bed file for whole exome (#61)
Greetings,
This error suggests that the system genReads.py is running on is unable to allocate the RAM required to store the reference sequence in memory. What kind of system are you running on? Are you trying to run all 23 jobs at once on the same computer (such that your memory is tasked with holding 23 copies of the reference sequences at a time?).
-Zach
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Hmm. I tried to replicate this but was unable to. (granted I used a different BED file to specify exome region: https://support.illumina.com/downloads/truseq-exome-product-files.html ) Are you able to track memory usage through an activity monitor, or something comparable, to see what its usage gets up to before dying? Is there anything particularly funky about the BED file you're using? If that file is publicly available (or if you don't mind sharing it with me) I could attempt to run the exact command on my end to see if there's a bug of some sort. |
Hi,
I tried the bed file from the link provided by you and it is working fine albeit taking long time for each job.
The bed file that I am using can be downloaded from Agilent’s SureDesign site. The design is SureSelectHuman All Exon V6 r2 and reference genome is hg19
Thanks
From: zstephens <[email protected]>
Sent: Friday, May 24, 2019 9:08 PM
To: zstephens/neat-genreads <[email protected]>
Cc: Mrinal Puranik <[email protected]>; Author <[email protected]>
Subject: Re: [zstephens/neat-genreads] Getting memory error while using hg19 as reference and targeted bed file for whole exome (#61)
Hmm. I tried to replicate this but was unable to. (granted I used a different BED file to specify exome region: https://support.illumina.com/downloads/truseq-exome-product-files.html )
Are you able to track memory usage through an activity monitor, or something comparable, to see what its usage gets up to before dying?
Is there anything particularly funky about the BED file you're using? If that file is publicly available (or if you don't mind sharing it with me) I could attempt to run the exact command on my end to see if there's a bug of some sort.
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Hi,
I am trying to simulate variants for whole exome with a targeted bed file. As per your suggestion, i divided the job into 23 jobs. However, i am getting error as shown below. Same error was generated when i tried with 50 and 100 as number of jobs. Would you please help me in resolving this error? I am using hg19.fasta as reference.
My command is:
python genReads.py -r hg19.fasta -R 75 -o hg19_allExon_simulated --pe 500 50 --vcf -t SSAllExon_V6_r2_S07604514_covered.bed -c 100 --job 2 23
And the error is:
Thanks
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