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The NCBI SRA ( Sequence Read Archive )


Contact: [email protected]
http://www.ncbi.nlm.nih.gov/Traces/sra/?view=toolkit_doc

The SRA Toolkit and SDK from NCBI is a collection of tools and libraries for
using data in the INSDC Sequence Read Archives.

Much of the data submitted these days, for example in BAM, Illumina export.txt,
and Complete Genomics formats, contain alignment information. With aligned data,
NCBI uses Compression by Reference, which only stores the differences in base
pairs between sequence data and the segment it aligns to.  The process to
restore original data, for example as FastQ, requires fast access to the
reference sequences that the original data was aligned to.  NCBI recommends that
SRA users dedicate local disk space to store references downloaded from the NCBI
SRA site.  As of Fall 2014, the complete collection of these reference sequences
is 66 GB.  While it isn't usually necessary to download the entirety of the
reference sequences, this should give you an idea of the scale of the storage
requirement.  By default, the Toolkit will download missing reference sequences
on demand and cache them in the user's home directory.  The location of this
cache is configurable, as is whether the download is automatic or manual.

For additional information on using, configuring, and building the toolkit,
please visit our web site at:

    http://www.ncbi.nlm.nih.gov/Traces/sra/?view=toolkit_doc&f=std


SRA Toolkit Development Team