Make confident decisions with trusted microarray solutions, from samples to insights
Please refer to below resources to make the most out of your prenatal research applications. Hear from current customers, watch webinars, blog posts and much more.
Webinars
Challenging microarray cases and the approaches for analysis of unusual findings
By Dr. Stuart Schwartz, Labcorp
Determining the genetic cause of disease by application of exon-level array as a complement to exome sequencing
By Dr. Benjamin Hilton, Greenwood Genetics Center
Case #1 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Catherine Rehder, Duke University
SNP Chromosomal Microarray, the allelic difference
By Dr. Elizabeth McCready, McMaster University
Case #2 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Kristen Deak, Duke University
Case #3 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Kristen Deak, Duke University
Using hybrid-SNP microarrays to delineate UPD in cytogenetic samples
Dr. Stuart Schwartz, Labcorp
Additional webinars
Clinical diagnosis of developmental disorders with chromosomal microarrays
Dr. Barbara DuPont, Senior Director, Cytogenetics Laboratory, Greenwood Genetic Center
CMA compares with conventional karyotyping in prenatal screening
Dr. Panyu Panburana, Dr. Takol Chareon-sirisuthigul and Dr. Thipwimol Tim-Aroon,Ramathibodi Hospital, Mahidol University
White papers
Literature
Infographics
Videos
GGC single exon deletion/duplication with CytoScan XON
Biallelic deletions of the Waardenburg II syndrome gene, SOX10, cause a recognizable arthrogryposis syndrome
Blog posts
Posters
Applications and technical resources
For Research Use Only. Not for use in diagnostic procedures.