BioRails DM
Screening to in vivo
All your data - safe, secure and searchable
BioRails DM is a comprehensive laboratory information management system designed to address a range of workflow driven research activities including
- Screening
- ADME
- In vivo research
- Safety toxicology
- Translational research
- Bioanalytical testing
It can be used to design flexible processes and workflows for capturing experimental data. This defines the procedures used to reliably capture high quality information. By separating design from execution BioRails DM provides separation between the plan and reality. This allows scientists to use the system across the full range of scientific investigations from routine activities such as ADME to more exploratory research such as in vivo behavioural studies. BioRails LIMS offers a much higher degree of flexibility than traditional LIMS or Data management solutions.
Workflow recipes - processes can be sequenced into a default workflow for an experiment allowing scientists to pre-plan and execute an experiment based on the default workflow.
Processes -every process has a default form associated with it for capturing both the data and the relationships between data. These can be completed directly in the web interface or templated in Microsoft Excel or Morphit for faster more accurate working.
SOP deployment - standard operating procedures, safety documentation and even processing templates are managed in the system and automatically deployed with the experiment to the scientists.

An example HTS Dose response process. Complex protocols can be distilled into simple re-usable process definitions used across many different assays.

The recipe defines the workflow for experiments allowing a whole experiment to be defined from a single method definition in one step.
Flexibility
- "Breadth first - simple process definitions can be defined using only a few high level parameters; the experiment folders are used to store files and documents containing information relevant to the activity
- "Depth first - parameters can be defined to capture all the information generated during a study, from the conditions used to the results generated, in a series of processes combined into an assay definition; raw data can be archived in the experiment and task folders together with analysis and reports; this can be supported by analysis templates used to automate activities and increase efficiency

