We’ve got some new and exciting updates this month! We’re proud to announce our collaboration with ThermoFisher for the integration of ChAS and Franklin. Check out the new features that aim to support microarray workflows from raw data, through variant analysis and interpretation, to reporting.
ChAS integration
Franklin has partnered with ThermoFisher to offer a comprehensive and robust solution for case interpretation, report generation, and team collaboration for all CytoScan microarray workflows. Molecular scientists and cytogeneticists can now enjoy the integration of their ChAS cases with Franklin, allowing them to easily import their segments into the platform and take advantage of our world-class variant interpretation tool for CNVs.
Head to Franklin’s Help Center to watch a quick video tutorial on how to seamlessly import and analyze your CytoScan cases in Franklin, and learn about all the platform’s variant interpretation tools available for CNVs. Segment classification has never been easier!
As with all other workflows, Franklin for microarray also provides tools for collaboration among team members and with other genetics experts worldwide, as well as effortless and straightforward reporting with our user-friendly Report Studio. To learn more about these features, check out the Franklin for CytoScan solution page.
Stay tuned for more information about the upcoming launch webinar organized by ThermoFisher - we'll be posting the details on our social media channels. In the meantime, save the date November 9th!
We hope you find these updates useful! We encourage you to give them a try and share your thoughts. We appreciate your feedback.
If you’re interested in learning more about these new features, or want to explore analyzing FASTQ files and exporting custom reports with Franklin Premium, feel free to schedule a call!
- The Franklin Team |