Changes between Initial Version and Version 1 of SOPs/qc_SRA

Timestamp:

08/19/20 16:29:48 (4 years ago)

Author:

gbell

Comment:

--

SOPs/qc_SRA

@@ +1 @@
+== Downloading and processing NCBI SRA files ==
+
+**SRA** (for Sequence Read Archive) is a NCBI binary format for short reads.
+
+It's thoroughly described in the [[http://www.ncbi.nlm.nih.gov/books/NBK47528/|SRA Handbook]]
+
+SRA files can be downloaded as compressed fastq in a web browser using [[https://ewels.github.io/sra-explorer/|SRA Explorer]].
+
+Processing SRA files requires the [[https://ncbi.github.io/sra-tools/|NCBI SRA Toolkit]], which is installed on our systems.
+
+The main command is **fastq-dump <SRA archive file>**, like
+
+''**fastq-dump SRR060751.sra**''
+
+If your reads are paired, by default the #1 and #2 reads will end up concatenated together in the same file.  
+To check if the SRA sample has paired reads or not, go to the [https://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=run_browser SRA Run browser], enter the sample ID, and look in the table under "Layout".
+
+To get matched paired reads into separate files, use a command like
+
+''**fastq-dump --split-3 SRR060751.sra**''
+
+This works the same as using the "--split-files", but "--split-3" puts unpaired reads (if any) into a third file.
+
+You can ask also for gzipped output instead of typical fastq:
+
+''**fastq-dump --split-3 --gzip SRR060751.sra**''
+
+See [[https://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=toolkit_doc&f=fastq-dump|Converting SRA format data into FASTQ]] for all program options.
+
+Note that a fastq file is about 4-5x larger than its corresponding SRA file.
+
+fastq-dump can be used to download/fetch the SRA file, or you can download (eg. using wget) the SRA file directly and then run fastq-dump to get the fastq file.  Downloading SRA file directly will avoid changing home dir path for large file (see below).
+
+'''Note:''' As of fastq-dump version 2.8.1, running fastq-dump will require the vdb-config to be set up correctly.  By default, downloaded/cache file is copied to the user's home directory, which is likely to run out of space.  Run,
+
+{{{
+vdb-config --restore-defaults
+vdb-config -i #use the GUI to enter a different location.  
+}}}
+
+Manually editing the file, $HOME/.ncbi/user-settings.mkfg, doesn't seem to work.  See [[https://ncbi.github.io/sra-tools/install_config.html | NCBI SRA Installation/Config]].  Other alternatives: i) simply symlink the NCBI directory in your home directory to somewhere else with larger storage, or ii) download the SRA file directly (eg. using wget) before using fastq-dump.
+
+{{{
+#download SRR4090409.sra (e.g. use wget) from SRA and convert to fastq
+fastq-dump SRR4090409.sra
+
+#download SRA file via fastq-dump (important: home directory or vdb-config file must be set up correctly), and convert to fastq
+fastq-dump SRR4090409
+}}}
+
+In order to '''download a list of SRA files''' from NCBI, it is convenient to use prefetch. 
+
+As mentioned in [[https://www.ncbi.nlm.nih.gov/sra/docs/sradownload/| SRA website ]], you can download list of Run accessions from search results page ([[https://www.ncbi.nlm.nih.gov/sra/?term=cancer |- Example offsite image]]) - select Runs of interest by clicking on the checkboxes, click on "Send To", "file", and select "Accession List" in the drop-down menu.
+
+Given a set of SRA files listed in a single column in the text file "SraAccList.txt" (e.g. SRR7623010, SRR7623011, etc.), the following command will download the entire set:
+
+{{{
+prefetch --option-file sraAccList.txt
+}}}
+
+This is current as of prefetch v. 2.9.3 (2.9.3-1).  Note that the default location for downloaded files is in your home directory under ~/ncbi/ncbi_public/sra.  With this default, one can quickly run out of space.  One solution to address this problem is to edit your ~/.ncbi/user-settings.mkfg file to include the following line:
+{{{
+/repository/user/main/public/root = "/destination/for/big/storage/here"
+}}}
+
+or point to the destination folder with -O 
+
+
+'''Download Metadata:'''
+When in your GEO series page, click on SRA link -> click on "Send to" on the top of the page -> check the "File" radiobutton, and select "RunInfo" in pull-down menu. This will generate a tabular SraRunInfo.csv file with metadata available for each Run.