PacBio data - problem with SRA toolkit

[ynwh]

That is really helpful. Thank you, Ray.

In my case SRR1284074, if use
#fastq-dump SRR1284074
Rejected 163480 SPOTS because SPOTLEN < 1
Read 163482 spots for SRR1284074
Written 2 spots for SRR1284074

Use "--table SEQUENCE" to dump SRR1284074, I still got 3 spots rejected.
#fastq-dump --table SEQUENCE SRR1284074
Rejected 3 SPOTS because SPOTLEN < 1
Read 163482 spots for SRR1284074
Written 163479 spots for SRR1284074

Any more suggestions or comments on this issue are very welcome.

Dear all,

Not sure if you have resolved your problem, but I had a similar problem with PacBio reads, but from a different data set. After reading this thread, I asked NCBI's Helpdesk and they explained to me that PacBio data is special in that multiple reads with a lot of errors are used to form consensus reads. It is these consensus reads that are output with no options to fastq-dump:

fastq-dump SRR2003880

If the raw reads are required, you need to supply the --table SEQUENCE option. i.e.,

fastq-dump --table SEQUENCE SRR2003880

I hope this helps someone!

Ray

[rwan]

Dear all,

Not sure if you have resolved your problem, but I had a similar problem with PacBio reads, but from a different data set. After reading this thread, I asked NCBI's Helpdesk and they explained to me that PacBio data is special in that multiple reads with a lot of errors are used to form consensus reads. It is these consensus reads that are output with no options to fastq-dump:

fastq-dump SRR2003880

If the raw reads are required, you need to supply the --table SEQUENCE option. i.e.,

fastq-dump --table SEQUENCE SRR2003880

I hope this helps someone!

Ray

[Retro]

We downloaded the ENA fatsq file. It is exactly what we get as result of the SRA toolkit. So probably only 46K sequences are usable. What is still unclear is why the NCBI archive website shows the "zero" reads as sequences, e.g. SRA|SRR2003880.1

[GenoMax]

ENA record appears to have the same number of spots: ftp://ftp.sra.ebi.ac.uk/vol1/fastq/S...03880.fastq.gz

[GenoMax]

It is possible that the download from SRA is corrupt. Best recourse there is to wait to hear back from SRA support. They generally fix these files based on my experience.

In the mean time, hdf5 files from the download tab is the original data from the submitter. It does not appear to contain the metadata.xml file that is required by SMRTportal so you may not be able to use the original files right away.

[Retro]

Thanks. But those reads show up in the NCBI website as not empty.

[GenoMax]

Fastq-dump appears to be rejecting reads because of this

"Rejected 117005 SPOTS because SPOTLEN < 1".

These reads appear to have no sequence.

You can confirm this yourself by doing

$ fastq-dump -M 0 -F SRR2003880

You can download the original HDF5 files for this record (using the "Download" tab) and verify if there are many 0 length sequences. You will need access to SMRTportal to properly process the raw data files.

[Retro]

I have problems getting fasta from PacBio SRA file using SRA toolkit. For example, file SRR2003880.sra should contain about 163K sequences, it yields only 46K and those do not correspond to the same names on NCBI SRA website. I can successfully process other PacBio files, and I am using the newest version of SRA toolkit with the following command line:

sratoolkit.2.4.5-2-win64/bin/fastq-dump.exe --fasta SRR2003880.sra

My best guess is that the upload of the data on NCBI SRA website was incorrect. They did not answer me yet. I would very appreciate anybody's help or opinion.

Thank you.