Description
Quantity: 24 Tokens
Unit Size: Each
• CytoScan Automated Interpretaion and Reporting (AIR) Tokens augment the visualizations of CNV gains, losses, and LOH with key clinical research interpretation information through the combination of Chromosome Analysis Suite (ChAS) Software and Franklin by Genoox
• ChAS Software supports analysis of CytoScan data and was developed with the input from leading cytogeneticists
• It is optimized for copy number (CN) and cytogenetics research analysis and reporting.
• Franklin by Genoox is an end-to-end research analysis of genetic sequenced data
• The platform enables users to develop and run a diverse range of tests for multiple genetic indications
• It allows users to focus on the clinical aspects of analyzing and interpreting a genetic research testAI-driven clinical interpretation
• ChAS users can upload data on Franklin, a one-stop shop presenting multiple annotations on the segment and gene level
• This includes a region browser showing gene annotations and regions within the variant, dosage sensitivity data, multiple predictors, and moreStay on track with clinical guidelines
• Each segment is classified in accordance with the most up-to-date ACMG classification clinical guidelines
• The system also provides a detailed explanation of the applied and unapplied criteria available for the evaluatorClinical-grade reporting
• CytoScan AIR Tokens enable ChAS users benefit from the Franklin Report Studio, a robust tool for authoring and issuing clinical-grade reports
• The report automatically captures all clinical data from the case, embedding interpreted variants along with their classification, clinical summary, and technical information
• An intuitive and simple-to-use interface enables laboratories to implement the various stages of clinical reporting evaluation and sign-offLaboratory clinical database management and expansion
• With CytoScan AIR Tokens, clinical researchers benefit from Franklin's knowledge base that enables them to develop and curate internal clinical databases consisting of observations, assessments, and linked evidence
• Historical cases can easily be imported from ChAS, applying advanced metrics such as the internal occurrence rate of gains and losses
• These are stored in the knowledge base to allow researchers to re-use curated information at their convenienceBe part of community driven cytogenetics research platform
• Franklin seamlessly correlates the laboratory database with hundreds of thousands of key pieces of evidence by leveraging the vast amount of curated data shared by more than 20,000 of Franklin’s community members
• Clinical researchers can enjoy more than 350,000 shared classifications of variants and advanced metrics
