Thank you
Hey guys,
I am going to aligning reads from GSE35641 (http://www.ncbi.nlm.nih.gov/Traces/sra/?view=search_seq_name&exp=SRX119208&run=&m=search&s=seq), on ecoli reference genome (NC_000913). There are 6 sra files in GEO which the least size is more than 2G. Do you know any way to download the files faster? I need many hours to download a file of them in fasta format
Thank you biostars
2 answers
Look at using aspera from the command line or, if you are using R, as described in sections 3.5 and 3.6 of the SRAdb vignette.
Yep, install Aspera and run it as follows:
ascp -i $KEY/asperaweb_id_dsa.openssh -k 1 -QT -l 200m \
anonftp@ftp-trace.ncbi.nlm.nih.gov:/sra/sra-instant/reads/ByRun/sra/SRR/SRR390/SRR390728/SRR390728.sra \ # url for the file
./ # save location
$KEY should point to the directory containing asperaweb_id_dsa.openssh (it will be in the installation directory). See instructions here.
Sorry, is the command the same for Windows? I am not familiar with unix/linux.
Thank you,
I did all the steps but said that remote host not specified.
On the other hand if at last I could download, I need fastq or fasta, then can I download in these format or just sra?
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