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Highly Sensitive Structural Variant Detection for Medical Genetics: A Comparison to the Standard of Care
This webinar on 9/18 will outline how a team at Radboud University Medical Center is assessing ultra-long read optical mapping on the Bionano Saphyr system to replace classical cytogenetics approaches in routine testing and for the discovery of novel structural variants with potential scientific, prognostic, or therapeutic value that are missed by standard approaches. Register Here |
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Automated Library Prep for the MCI Advantage Cancer Panel
This poster from Beckman Coulter describes the automation of the MCI Advantage Cancer Panel at Miami Cancer Institute, a 170 gene panel assay based upon the Illumina TruSight Tumor 170 Panel, on the Beckman Coulter Biomek i5 Span-8 NGS Workstation. Download it from GenomeWeb’s White Paper Channel. |
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