Question: Downloading SRA data using the SRA Toolkit
0
gravatar for F
3.9 years ago by
F3.4k
Iran
F3.4k wrote:

Hey,

i opened cmd and typed C:\Users\yang\Downloads\Compressed\sratoolkit.2.5.0-win64\bin

then i typed fastq-dump -X 5 -Z SRR390728

in cmd i am watching

C:\Users\yang\Downloads\Compressed\sratoolkit.2.5.0-win64\bin\fastq-dump -X 5 -Z

SRR390728
Read 5 spots for SRR390728
Written 5 spots for SRR390728
@SRR390728.1 1 length=72
CATTCTTCACGTAGTTCTCGAGCCTTGGTTTTCAGCGATGGAGAATGACTTTGACAAGCTGAGAGAAGNTNC
+SRR390728.1 1 length=72
;;;;;;;;;;;;;;;;;;;;;;;;;;;9;;665142;;;;;;;;;;;;;;;;;;;;;;;;;;;;;96;;;;(
@SRR390728.2 2 length=72
AAGTAGGTCTCGTCTGTGTTTTCTACGAGCTTGTGTTCCAGCTGACCCACTCCCTGGGTGGGGGGACTGGGT
+SRR390728.2 2 length=72
;;;;;;;;;;;;;;;;;4;;;;3;393.1+4;;5;;;;;;;;;;;;;;;;;;;;;;;;9;;;;;;;464262

(.....)

where i can find the downloaded file???? i was going to download a sra file from GEO.

sequencing rna-seq • 2.2k views
ADD COMMENTlink modified 5 weeks ago by ATpoint15k • written 3.9 years ago by F3.4k
1
gravatar for genomax
5 weeks ago by
genomax65k
United States
genomax65k wrote:

Since this old thread has been re-activated I will add two current methods that should be used for this purpose instead of using SRAtoolkit:

ADD COMMENTlink modified 5 weeks ago • written 5 weeks ago by genomax65k

genomax as you suggested to me already, Fast download of FASTQ files from the European Nucleotide Archive (ENA) is quite applicable

ADD REPLYlink modified 5 weeks ago by ATpoint15k • written 5 weeks ago by F3.4k

This tutorial also contains a section on how to use the sratoolkit (prefetch and fastq-dump) efficiently (bottom of the tutorial).

ADD REPLYlink written 5 weeks ago by ATpoint15k
0
gravatar for Devon Ryan
3.9 years ago by
Devon Ryan89k
Freiburg, Germany
Devon Ryan89k wrote:

While you could download the file from GEO (or just directly from SRA), it would seem easier to just remove the -Z option and allow fastq-dump to write the fastq files for you. Exceedingly few programs directly accept SRA files, but pretty much everything will take fastq.

BTW, that's a paired-end dataset, so make sure you specify --split-files.

ADD COMMENTlink written 3.9 years ago by Devon Ryan89k

By default (now in 2019), one should use --split-3 to separate potential singletons that might mess up the pairwise structure of the two mate fastq files which eventually might crash the aligner.

ADD REPLYlink modified 5 weeks ago • written 5 weeks ago by ATpoint15k
0
gravatar for cigdemselli
5 weeks ago by
cigdemselli0 wrote:

The default location for the "download repository" is:

Linux: /home/[user_name]/ncbi/public
Mac OS X: /Users/[user_name]/ncbi/public
Windows: C:\Users\[user_name]\ncbi\public

Please see this link for more details: https://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=toolkit_doc&f=std#s-4

ADD COMMENTlink modified 5 weeks ago by ATpoint15k • written 5 weeks ago by cigdemselli0

Hi, welcome to Biostars :)

Please use the formatting bar to indicate code examples, paths, example data etc. I did the changes for you this time.

enter image description here

ADD REPLYlink modified 5 weeks ago • written 5 weeks ago by ATpoint15k
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