Contrary to the semiconductor industry where investments in
excess of $1 billion are needed to setup a fabrication plant, most synthetic
biology projects rely on low-cost instruments and infrastructure commonly
available to life scientists. What distinguishes a synthetic biology laboratory from a regular
biological research laboratory is the application of engineering methods to
develop DNA molecules meeting user-defined specifications. In particular, the
life cycle of a synthetic biology project is generally broken down into three
phases: design, fabrication, and testing. Unfortunately, only a very limited
number of research groups and scientists have the breadth of expertise
necessary to address the numerous scientific and technical challenges raised by
each stage of a synthetic biology project. Some argue that progress in
synthetic biology has been hampered by the lack of software tools allowing
projects to move smoothly through the different stages of the design-build-test
cycle. It is our opinion that synthetic biology is a very young engineering
specialty still in search of its own paradigms. While there have been analogies
made with microelectronics, software, and other mature engineering fields, no
practical solutions exist to synthetic biology’s daunting scientific challenges
today.

Several companies (Amyris, Intrexon) and government-funded
labs (JBEI) have invested in the development of enterprise systems necessary to
scale up their Research and Development (R&D) effort by building large
teams composed of more specialized technical staff focused on a particular
stage of the project. Unfortunately, the products of these multimillion dollar
investments are proprietary infrastructures in which the underlying software is
tightly coupled to specific manufacturing and test technologies. These facilities
give their owners a competitive advantage but do little to promote the
dissemination of engineering methods in the life sciences.
Rather than developing a one-of-a-kind facility, our vision
is to catalyze a transformation of our national life science
R&D infrastructure into a network of
individual labs, core facilities, consortiums, small and larger biotech
companies, and government laboratories. This can be achieved through the
development of an integrated suite of software tools facilitating the design of
synthetic DNA molecules (GenoCAD), their assembly through de novo synthesis and reuse of existing components (GenoCAM), the
characterization of their dynamics in vivo (GenoSIGHT), while monitoring for the
possible presence in the pipeline of sequences that may raise biosecurity or
biosafety concerns (GenoGUARD). We call Genetic Design Automation (GDA) the
integration of tools that span the entire design-build-test workflow; the tool
chain resulting from the integration of GenoCAD, GenoCAM, GenoSIGHT, and
GenoGUARD is called GenoGDA. 
The GenoGDA applications are at different stages of development. Ultimately they will all have graphical user interfaces
friendly to life scientists who do not have any engineering background. Their
deployment will be facilitated by their client-server architecture and the use
of web technologies that do not require the installation and support of
stand-alone applications. They will be licensed open source and available from
SourceForge allowing users to install them on their own servers. We acknowledge
that the installation of all the software components may be challenging and
expensive, possibly beyond the capabilities of some potential users. Thus, in
order to reduce the cost of deployment while maximizing the computing
performance, the software suite will also be made available preinstalled on
High-Performance Computing (HPC) hardware designed to optimize the GDA
computing workflows. We call the combination GDA software and custom hardware
an HPC appliance.  |