download it again.
hello.
I encountered an error during the execution of the fastq-dump using the SRA data.
(SRA data : SRR1597832, SRR1597841 etc...)
first error message is as follows:
2015-01-27T09:40:46 fastq-dump.2.4.3 err: binary large object corrupt while reading binary large object within virtual database module - failed
I'm use command :
fastq-dump --split-3 SRR1597832.sra
In order to solve this problem.....................
1. SRR1597832 data Re-download
URL: ftp://ftp.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR159/SRR1597832/
The error message is as follows:
G:\sratoolkit.2.4.3-win64\bin>fastq-dump --split-files SRR1597832.sra
2015-01-29T09:15:39 fastq-dump.2.4.3 err: binary large object corrupt while read
ing binary large object within virtual database module - failed SRR1597832.sra
=============================================================
An error occurred during processing.
A report was generated into the file 'C:\Users\Administrator/ncbi_error_report.x
ml'.
If the problem persists, you may consider sending the file
to 'sra@ncbi.nlm.nih.gov' for assistance.
=============================================================
2. command change
The error message is as follows:
G:\sratoolkit.2.4.3-win64\bin>fastq-dump --split-files SRR1597832
2015-01-29T08:27:41 fastq-dump.2.4.3 err: buffer insufficient while executing fu
nction within transform module - failed SRR1597832
=============================================================
An error occurred during processing.
A report was generated into the file 'C:\Users\Administrator/ncbi_error_report.x
ml'.
If the problem persists, you may consider sending the file
to 'sra@ncbi.nlm.nih.gov' for assistance.
=============================================================
It is not possible to solve the problem.
Please help me.....
Please answer fast.
Thank you.
5 answers
My understanding is that there is a networking error, and the situation is expected to be remedied by Monday.
If it's not playing ball, just get the fastq files directly:
ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/002/SRR1597832/
That's generally easier than getting the sra files and then using the slow dump command anyway :p
NCBI SRR1597832 data fastq-dump program result data and the result is the same data?
A new version (2.4.4) of the sra toolkit has been released!
Thank you!
download new release..
The NCBI SRA is definitely acting strangely. Earlier today I was having similar issues. If you absolutely need the data right now you should be able to download the entire .sra file from the NCBI FTP site. It seems that the SRA Toolkit API for fetching archives is not working properly today...
download it again.
Are you asking people to download it again or are you saying you downloaded it again?
sorry.
I'm downloading the data again
ftp://ftp.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR159/SRR1597832/
The reason you are getting the error is the deposited SRA file is in bam format and you would have to add the genome file to it.
Please take a look at
http://www.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=toolkit_doc&f=std
One option is to download the fastq file and directly follow the pipeline. On some exome sequencing data fastq dump doesnt work as efficiently or gives errors as the deposited data is in bam format and requires genome file. So from the below website we can directly download the fastq files for all sequencing experiments in GEO.
I guess OP's problem was solved when OP tried re-downloading the files.
Thank you.
I was already using the method proposed by you.(vdb-config)
However, continuing an error occurs.
Thanks for the URL.
thank you.
Add file: prj_phs710EA_test.ngc
Log in to answer this question.
Please paste the contents of the
ncbi_error_report.xmlfile so we can help you.Thank you for answers.
ncbi_error_report.xmlfile:Moved to GitHub-Gist here:
I'm not sure what the problem is. While you're waiting for answers here, you should also email the XML file to sra@ncbi.nlm.nih.gov.
Already sent an e-mail.
Answer mail information.................
Still not resolved.
What is your machine configuration in terms of RAM?
My computer operating system Window 7 64bit.
Computer RAM 32.0GB.
Hmmm, let's try this possible solution: Open
G:\sratoolkit.2.4.3-win64\binand right click on fastq-dump, choose Properties. See if you have an Unblock option (like the one shown here). If you see it, unblock and hit OK. Try the command again and check if the error persists.Hmmm.....Check the results are not visible...
instead, set the compatibility mode. win7.
Currently running again.