Microarray for Postnatal Genetic Research Resources

Reproducible results with powerful microarray analysis

Please refer to below resources to make the most out of your 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

 

SNP Chromosomal Microarray, the allelic difference

By Dr. Elizabeth McCready, McMaster University

 

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

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

Videos

Current Time 0:00
Duration 6:17
Loaded: 0%
Stream Type LIVE
Remaining Time 6:17
 
1x
    • Chapters
    • descriptions off, selected
    • captions off, selected
    • en (Main), selected

    GGC single exon deletion/duplication with CytoScan XON

    Current Time 0:00
    Duration 2:44
    Loaded: 0%
    Stream Type LIVE
    Remaining Time 2:44
     
    1x
      • Chapters
      • descriptions off, selected
      • captions off, selected
      • en (Main), selected

      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

      Bleach protocol recommendation for CytoScan assays

      Bringing Artificial Intelligence and Automation to Genetic Analysis

      Bringing Artificial Intelligence and Automation to Genetic Analysis

      Improved understanding of fetal abnormalities with CytoScan XON and exome sequencing

      Bleach protocol recommendation for CytoScan assays

      Which cytogenetic technique Is right for you?

      Bleach protocol recommendation for CytoScan assays

      Uncovering the genetics behind autism spectrum disorder

      Bleach protocol recommendation for CytoScan assays

      History and evolution of cytogenetics

      Bleach protocol recommendation for CytoScan assays

      SNP detection tools

      Bleach protocol recommendation for CytoScan assays

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

      Bleach protocol recommendation for CytoScan assays

      Posters

      Characterization of exon-level genomic copy number changes

      Bleach protocol recommendation for CytoScan assays

      Exon-level detection of human copy number variation

      Bleach protocol recommendation for CytoScan assays

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

      Bleach protocol recommendation for CytoScan assays

      Applications and technical resources

      Bleach protocol recommendation for CytoScan assays

      Bleach protocol recommendation for CytoScan assays

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

      Bleach protocol recommendation for CytoScan assays

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