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9.0 years ago
ywwangkevin
•
0
I am trying to convert .sra files to fastq using fastq-dump in Ubuntu. I have already downloaded the sra files. I used the command:
fastq-dump --split-files /home/ywwang/ncbi/public/sra/GSE52643/SRR1035695.sra
and I got the information below:
Read 33108579 spots for /home/ywwang/ncbi/public/sra/GSE52643/SRR1035695.sra
Written 33108579 spots for /home/ywwang/ncbi/public/sra/GSE52643/SRR1035695.sra
Does it mean the program have converted the sra file successfully? But I couldn't find the output file
Thanks, Antonio. I just couldn't find the output file if I used the command above.But I tried add output path to command and it worked. Does the program output file to the path where input file located if I use the command with no output path like above?
Hi, I am new to NGS and I am trying to convert .sra files into .fastq by the following command
but it is not working and giving an error by generating an error file... what should I do now