High-content screening (HCS) technologies are becoming increasingly used in both large-scale
drug discovery and basic research programs. These automated imaging and analysis technologies
enable the researcher to elucidate the complex biology that underlies the functions
of genes, proteins, and other biomolecules at the cellular level. HCS combines the
power of automated digital microscopy and advanced software-based image analysis algorithms
to detect and quantify biological changes in cells and tissues. This technology is
a particularly powerful tool when used to interrogate the cellular effects of exogenously
applied agents such as RNAi and/or small molecules. HCS allows for the evaluation
of cellular perturbations that occur both at the level of the single cell and within
cellular populations. In a multivariate approach, multiple cellular parameters are
collected, allowing for more complex analysis. However, in these scenarios, data flow
and management still represent substantial bottlenecks in HCS projects. HCS data include
a diversity of information from multiple sources such as details pertaining to screening
libraries (e.g., siRNA and small molecules), image stacks acquired from automated
microscopes (of which there may be up to several million), and the image analysis
data. From this, postprocessing algorithms are required to generate statistical, quality
control bioinformatic information and ultimately a final hit list. To accomplish these
individual tasks, numerous tools can be used to perform each analytical step; however,
management of the entire information flow currently requires the use of commercially
available proprietary software, the scope of which is often limited, or bespoke customized
scripts. In this article, the authors introduce an open-source research tool that
allows for the management of the entire data flow of the HCS data chain, by handling
and linking information and providing many powerful postprocessing and visualization
tools. (Journal of Biomolecular Screening 2010:892-899)
