Microarray Solutions for Prenatal Genetic Research Resources

Make confident decisions with trusted microarray solutions, from samples to insights

Please refer to below resources to make the most out of your prenatal and postnatal 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

Videos

GGC single exon deletion/duplication with CytoScan XON

Biallelic deletions of the Waardenburg II syndrome gene, SOX10, cause a recognizable arthrogryposis syndrome

CytoScan Automated Interpretation and Reporting Demo

Blog posts

Choosing a genetic analysis method for your research laboratory

Bringing Artificial Intelligence and Automation to Genetic Analysis

Hybrid-SNP Microarrays for Uniparental Disomy

Choosing a genetic analysis method for your research laboratory

Hybrid-SNP Microarrays for Uniparental Disomy

Using high-density DNA oligonucleotide arrays to detect copy number variations in human disease

Improved understanding of fetal abnormalities with CytoScan XON and exome sequencing

Uncovering the genetics behind autism spectrum disorder

Which cytogenetic technique Is right for you?

History and evolution of cytogenetics

SNP detection tools

Solving gene puzzles with the CytoScan: An interview with Barb DuPont

Posters

Characterization of exon-level genomic copy number changes

Exon-level detection of human copy number variation

Customized copy number analysis of pre-and postnatal samples using Chromosome Analysis Suite (ChAS) software

Applications and technical resources

Bleach protocol recommendation for CytoScan assays

Overcoming challenges in reproductive health applications by deploying more sensitive and accurate molecular technologies

For Research Use Only. Not for use in diagnostic procedures.