Significance Associated with Phenotype (SAP) Score: A Method for Ranking Genes and Genomic Regions Based on Patient’s Phenotype
Video
Benefits of migrating from GRCh37 to GRCh38 for CNV analysis and reporting – a panel discussion with clinical genomics experts
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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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CGC 2020 Poster Presentation: Unique Cancer Cytogenetics Knowledgebase Integrated with a Machine Learning System to Improve Quality and Utility of Clinical Reports
Video
Genome sequencing reveals cause of multi-generational split hand/split foot with long bone deficiency
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