Implementing high-throughput cloud-based microarray analysis in the UK Genomic Medicine service
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Demonstrating How You Can Obtain More Answers from Your NGS Data by Using Bionano’s NxClinical Software
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Tutorial: UPD Detection from SNP arrays or NGS data (10 mins)
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Rapid implementation of the latest technical standards with the NxClinical integrated ACMG scoreboard
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Copy Number Variant Detection by NGS: Coverage, Uniformity & Resolution
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Detection of CNV and AOH from NGS Data Tutorial
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ACC 2021 Poster Presentation: Comparison of different SNP microarray designs and WGS for cytogenetic testing
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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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