jean.elbers Thanks for pointing these errors to me.. part of which just got introduced when I wrote this post. Now it seems like its creating fastq files, but unfortunately also creating some strange error:
./fastq-dump : 2.9.0
2018-05-24T12:10:07 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path '1' cannot be opened as database or table
2018-05-24T12:10:07 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path 'medsmit' cannot be opened as database or table
2018-05-24T12:10:08 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path 'staff' cannot be opened as database or table
2018-05-24T12:10:08 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path '25754388' cannot be opened as database or table
2018-05-24T12:10:08 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path '18' cannot be opened as database or table
2018-05-24T12:10:08 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path 'May' cannot be opened as database or table
2018-05-24T12:10:08 fastq-dump.2.9.0 err: item not found while constructing within virtual database module - the path '15:16' cannot be opened as database or table
Read 134818 spots for /Users/medsmit/ncbi/public/sra/SRR3502002.sra
Written 134818 spots for /Users/medsmit/ncbi/public/sra/SRR3502002.sra
Trying to understand why are they there . Thanks,
Do you have a space between
--andsplit-filesin the loop? I would also usels -1so only one file is fed tofastq-dumpfor each iteration of the loop.Thanks Genomax. Yes I do have space between -- and split-files in the loop. Also I tried with ls -l After I pass this code bellow:
I only see
As if it entered in any interface. Not sure what wrong I am doing. Thanks, Suparna
You can't have a space between
--split-files. That was also a1(number one) notl(L) in thelscommand.And two additional mistakes noted by @jean below.
Alternatively, you can always check the ENA for your files, which are typically mirrored there directly as fastq, or use parallel-fastq-dump (python3) if the sra files are big (tens of Gb).