Success in science hinges upon data, and data generation is dependent upon speed and quality. In turn, speed and quality are dependent on how you process samples. Manual processing is wrought with time-consuming bottlenecks and risks of error and variation.
Automated systems offer precise, accurate high-throughput processing, but so many of these systems are limited to single protocol processing. This imposes a defined cap on overall discovery and sample processing speed. In some cases, labs may opt to purchase additional hardware, which takes up precious lab space and burns through capital as well as ongoing maintenance funds.
Instead, parallel processing enables multiple, different assays to be run at once on a single automated system. By doing so, labs can maximize sample processing throughput and rapidly reap insight-generating data without sacrificing quality. The speed and quality empower today’s savvy research organizations, especially those in drug discovery and genomics, to achieve new heights of success faster than their competitors.
On top of this, parallel processing enables researchers to address diverse experiments, with dissimilar parameters, conditions, and samples, more efficiently than single processing. Assay replicates and controls can be run in parallel to improve statistical validity and data quality. This minimizes experimental variability and improves reproducibility, especially in applications where accuracy and consistency are critical yet fragile.
Devices are not the only factor to consider when seeking to increase speed and quality through parallel processing. In fact, hardware, software, and peopleware comprise a three-pronged approach to automation. Learn more about this approach in our blog, “Lab Automation’s Cogent Trichotomy”.
With that said, the limitations of single protocol processing may often be a factor of the automated system’s scheduling software. In fact, many software packages can schedule a simple, single biochemical assay, but very few can run simultaneous protocols in parallel. Impacts may manifest downstream as increased waiting time for data to drive an analysis cycle.
The right software, such as Cellario whole lab automation software, can facilitate single and parallel processing as the needs arise. And it can grow and change along with your evolving needs.
What’s more, the automation and scheduling software should support quality data through adherence to FAIR Principles published by GO FAIR. These principles aim to improve scientific data management and stewardship in the Digital Age, especially analytical, event-based, and meta data harvested from automated systems. In essence, data should be findable, accessible, interoperable, and reusable.
Parallel processing is necessary to convert your lab into a highly functional data factory. In addition to evaluating hardware, it’s important to conduct due diligence on the system’s scheduling and management software to be sure that it can perform to your current and future expectations. As you define your requirements and evaluate options, here are some factors to consider.
And of course, a hands-on demonstration is extremely useful to truly gauge the software’s utility and ease of operation in context of your lab’s needs.
Parallel processing is a critical capability as it improves the efficiency of sample processing and resource utilization, reduces time to discovery, and speeds your lab’s ability to discover and generate data. In turn, you can identify targets faster, present findings earlier than your competition, and achieve new heights of success.
To learn more about parallel processing, read our blog, “Parallel Processing: The Key to Productivity and Fast Results”.
And as you enter advanced discussions with an automated system scheduling and management software provider, consider asking these final questions:
As always, we welcome you to connect with us to learn more about Cellario whole lab automation software. We’re happy to answer the aforementioned questions and many more, and we look forward to providing you with a personalized demonstration.
Revision: BL-DIG-230714-01_RevA