Figure 1.
Overview of the STORMSeq system.
The user uploads short reads to Amazon S3 and starts a webserver on Amazon EC2, which controls the mapping and variant calling pipeline. Progress can be monitored on the webserver and results are uploaded to persistent storage on Amazon S3.
Figure 2.
STORMSeq provides basic visualization for summary statistics, such as (A) genome-wide SNP density and (B) size distribution of short indels.
Table 1.
Approximate costs for STORMSeq.