Unconfigured Ad
Collapse
X
-
Solve the problem
Try "fastq-dump --split-files ./library.sra".Originally posted by ALB_1 View PostHi there, I am trying to use fastq-dump on an sra file downloaded from NCBI GEO and keep getting the error message:
err: name not found while resolving tree within virtual file system module - failed to open 'SRRfilenamehere'
Written 0 spots total
I downloaded the correct version and have used this toolkit successfully on other computers. Could it be an installation issue? Thank you!
It is works.
Leave a comment:
-
This is an ongoing case study in why you should just stick with sftp and gzip.
A camel is a horse designed by a committee and this SRA compression and decryption is a real camel.
Leave a comment:
-
I was having the same issue. Specifying the full path worked for me too. Thanks!
Kevin
Leave a comment:
-
This finally worked for me. The home mounted via NFS was not an issue. I also discovered that trying to change the default ncbi directory caused a lot issues, as a ~/ncbi directory was created after adding an encrypted repository. That is also where the refseq files have to go, even if the root is elsewhere. Basically leave the ncbi root in your home directory, and add the refseq files there.Originally posted by genomeHunter View PostI think I have finally found the solution!
Some new SRA files need refseq for dumping. It should be in ~/ncbi/public/refseq (default path). For some reason, my SRA toolkit was unable to download them, so I manually downloaded them from
ftp://ftp-trace.ncbi.nlm.nih.gov/sra/refseq/
Try running 'vdb-validate' and 'test-sra +a' to see which sequences you need to download.
Cheers
GH
PS. SRA technical staff are friendly and knowledgable. Contact them if the problem persists! :-)
Leave a comment:
-
I had this issue as well and providing the absolute path was not resolving it. In the end I found that the error (virtual file system) had to do with the machine not having web access. Copying the required reference files into: /yourhomedir/ncbi/public/refseq solved it.
Leave a comment:
-
Guys,
the problem happens when you use a local path for the SRA file. Try using the absolute path! fastq-dump /data/etc/SRR00000.sra should do the trick
Leave a comment:
-
Solution
I think I have finally found the solution!
Some new SRA files need refseq for dumping. It should be in ~/ncbi/public/refseq (default path). For some reason, my SRA toolkit was unable to download them, so I manually downloaded them from
ftp://ftp-trace.ncbi.nlm.nih.gov/sra/refseq/
Try running 'vdb-validate' and 'test-sra +a' to see which sequences you need to download.
Cheers
GH
PS. SRA technical staff are friendly and knowledgable. Contact them if the problem persists! :-)
Leave a comment:
-
I have tried everything, in every forum, and in every thread.Originally posted by GenoMax View PostTry to run the "configuration-assistant.perl" that is present in the "bin" directory.
While you are running the perl script you will reach a point where the software asks you "Would you like to test SRA files for remote reference dependencies? [y/N]". Choose "Yes" (default answer is No) which will then prompt you to provide an SRA accession number. Try providing the SRA# you are having problems with and see if the script downloads the right reference files.
Try "fastq-dump"ing that SRA file.
There is also a possibility that some SRA files may be corrupt or otherwise problematic (happened with one I was interested in). You may want to ask SRA support to check on the problematic accession #'s.
I simply cannot understand why such a presumably simple and tiny application could cause so much headache. It just cannot be solved
Last thing I tried, without success:
GH
Leave a comment:
-
Try to run the "configuration-assistant.perl" that is present in the "bin" directory.Originally posted by genomeHunter View Post
Any ideas?
Cheers
GH
While you are running the perl script you will reach a point where the software asks you "Would you like to test SRA files for remote reference dependencies? [y/N]". Choose "Yes" (default answer is No) which will then prompt you to provide an SRA accession number. Try providing the SRA# you are having problems with and see if the script downloads the right reference files.
Try "fastq-dump"ing that SRA file.
There is also a possibility that some SRA files may be corrupt or otherwise problematic (happened with one I was interested in). You may want to ask SRA support to check on the problematic accession #'s.
Leave a comment:
-
Hello,
I am also trying to dump the new reference-based SRA files. It has been driving me nuts, as it is impossible to get to work. Some NBCI staff are very friendly and are trying to help but it all has been fruitless.
Things I have found out till now:
- For some reason, the toolkit is unable to download the refseq so I manually downloaded them from ftp://ftp-trace.ncbi.nlm.nih.gov/sra/refseq/ and put them in "~/ncbi/public/refseq" (the working directory set when using the sratoolkit.jar setup)
- 'test-sra' and 'vdb-validate' can be used for verifying the consistency of SRA files
- fastq-dump works for some files (after manually downloading the refseq files) and does not work for some others with the following ambiguous error message:
Any ideas?VResolverAlgRemoteResolve: name not found while resolving tree within virtual file system module - failed to open
Cheers
GH
Leave a comment:
-
I am curious to know if the SRA file you were interested in employed reference based compression or not?Originally posted by crazyhottommy View PostYes, feed the full path of your sra file to sam-dump resolved my problem also.
The original discussion had started with reference to "reference compression based files" which require a one time local storage configuration via the perl script or java file.
Leave a comment:
-
Originally posted by chenz123 View PostI had the exact same problem, and apparently the solution is very simple, according to this Czech Wiki site : (https://wiki.metacentrum.cz/wiki/SRA...it_application) you need to execute the fastq-dump command while typing the full path to the SRA file.
for me, it worked like magic.
Cheers.
Chen.
Yes, feed the full path of your sra file to sam-dump resolved my problem also.
Leave a comment:
-
I had the exact same problem, and apparently the solution is very simple, according to this Czech Wiki site : (https://wiki.metacentrum.cz/wiki/SRA...it_application) you need to execute the fastq-dump command while typing the full path to the SRA file.
for me, it worked like magic.
Cheers.
Chen.Last edited by chenz123; 04-28-2013, 01:52 PM.
Leave a comment:
-
There is. Unfortunately the settings file has to be manually modified. You can either email SRA support or I can help off-line.Originally posted by Susanna5 View PostThanks very much for responding, and so quickly! Your suspicion is correct, my HOME is mounted via NFS. So, if I understand this correctly, there is no way to download data from the SRA for my situation? I am running windows actually, but from the SRAtoolkit guide, I understood that it was only for linux and Amazon Cloud. I'm a bit confused about your other comment over windows, but perhaps that is with NCBI Decryption Tools?
SRA-tookit is available for windows (http://ftp-trace.ncbi.nlm.nih.gov/sr....2-4-win64.zip) but only for 64-bit. If you have 64-bit windows than get the installer and then follow the directions I posted in #6.
Leave a comment:
Latest Articles
Collapse
-
by SEQadmin2
CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
Despite this, “CRISPR helped turn genome editing from a specialized technique into...-
Channel: Articles
07-31-2026, 11:01 AM -
-
by SEQadmin2
Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.
The systematic characterization of the human proteome has...-
Channel: Articles
07-20-2026, 11:48 AM -
-
by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
...-
Channel: Articles
07-09-2026, 11:10 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 08-03-2026, 10:13 AM
|
0 responses
15 views
0 reactions
|
Last Post
by SEQadmin2
08-03-2026, 10:13 AM
|
||
|
Started by SEQadmin2, 07-31-2026, 02:55 AM
|
0 responses
32 views
0 reactions
|
Last Post
by SEQadmin2
07-31-2026, 02:55 AM
|
||
|
Started by SEQadmin2, 07-24-2026, 12:17 PM
|
0 responses
23 views
0 reactions
|
Last Post
by SEQadmin2
07-24-2026, 12:17 PM
|
||
|
Started by SEQadmin2, 07-23-2026, 11:41 AM
|
0 responses
21 views
0 reactions
|
Last Post
by SEQadmin2
07-23-2026, 11:41 AM
|
Leave a comment: