BioDiscovery Webinars
Choose by Resource, then filter by Product OR Topic
This webinar is geared towards those involved with genomic variation analysis and interpretation of homologous recombination deficiency (HRD) from microarray data or next-generation sequencing (NGS) data in cytogenetics, molecular pathology, or molecular genetics labs.
This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from microarray data in cytogenetics or molecular genetics labs.
This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from next-generation sequencing (NGS) data in cytogenetics or molecular genetics labs.
This webinar is geared towards those involved with genomic variation analysis and interpretation of microarray and sequencing data in cytogenetics or molecular genetics labs.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Analyzing copy number variation in cancer tissues can be a difficult task, but Nexus Copy Number can help!
Learn how to identify relevant common events within the TCGA project and how to leverage the clinical information provided for the samples.