CGC 2020 Poster Presentation: Unique Cancer Cytogenetics Knowledgebase Integrated with a Machine Learning System to Improve Quality and Utility of Clinical Reports
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Genome sequencing reveals cause of multi-generational split hand/split foot with long bone deficiency
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Real-world experience utilizing NxClinical for CNV detection using standard-of-care testing in Post-natal specimens
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Embracing the power of the SNP. NxClinical facilitates detection of UPD and determination of parent of origin from SNP microarray data.
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An unorthodox journey and our experience for validation of NxClinical and the GSA Beadchip microarray
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Tutorial: Modern CMA Solutions: New GDA-Cyto and GSA-Cyto SNP arrays with NxClinical (30 mins)
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Tutorial: Combinatorial analysis of Copy Number and Sequence Variants at your fingertips (30 mins)
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Tutorial: Copy Number analysis by NGS: Urban legend or true reality? (30 mins)
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Tutorial: What is NxClinical and how can it help my case review? (30 mins)
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Tutorial: Building and using Gene & Region Panels in NxClinical (10 mins)
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Tutorial: Inheritance analysis using array or NGS data (30 mins)
