- SeqOne's CE-IVD platform now provides an interpretation solution for Agilent’s MicroArrays CGH users.
- SeqOne CGH Array solution enables a seamless transition, including historical data import, from discontinued Cartagenia bench lab software.
- We offer free trial testing of the SeqOne CGH Array solution.
At SeqOne, our interpretation platforms powered by explainable AI prediction algorithms can assist biologists in performing fast and reliable interpretation at scale.
We are excited to bring together in one CE-IVD cloud environment Array and NGS analysis across a wide range of applications: germline tests (Panel, WES & WES) and Somatic applications (Small /large Panels, Hemato, ct-DNA, solid tumors, drug recommendation, MSI/TMB/HRD signatures, etc.).
Annotate and Classify with Precision with direct import of CNV data from Agilent’s Cytogenomics software (IntervalBasedReport files), transforming raw data into actionable insights.
Each CNV is meticulously annotated and classified, drawing from a rich array of genomic databases and resources, including DGV, GnomAD annotations, OMIM transmissions & clinical regions, Decipher HI and TriploInsufficiency scores, internal frequency database, CNV knowledge base, and more.
Automated ACMG Classification directly integrated into the CNV Viewer, streamlining the interpretation process. Easy access to ACMG classification results, with detailed insights into the criteria utilized for classification.
Tailored Filters for Precision Analysis: including sample-frequency, enabling the exclusion of frequent CNVs within personal cohorts. Also filters to select OMIM Morbid genes and let you filter on the CNV Size. CNV can be sorted on various options, and by default we provide a sort on the ACMG automatic classification.
Import your Knowledge base and historical analysis: We freely import your knowledge base to SeqOne with all your previous annotations and classifications. This information is available in your own “Variant Knowledge Base” in SeqOne, providing detailed information about all overlapping CNV that you have annotated in the past, with class and comments.
& much more to come… we are hard at work, listening to our Customers to determine how we can best continuously improve SeqOne functionalities and user experience.
See SeqOne CGH Array in action
If you are looking for a new CGH Array interpretation solution do not hesitate to contact us. We would be delighted to give you a demo.
About SeqOne
SeqOne is a leading European provider of AI-powered software for next-generation sequencing (NGS) data analysis in oncology and rare diseases. Its cloud-based platform transforms complex genomic data into fast, precise, and actionable insights, supporting molecular labs in delivering life-saving diagnoses and treatments. The SeqOne Platform is a CE-IVD Class C certified under IVDR in vitro diagnostic medical device. Driven by the vision of personalized medicine for every patient, everywhere, SeqOne is scaling the future of genomic medicine—one lab at a time.
For more information, visit seqone.com.
