Laboratory genetics and genomics

729 - Practice Convergence in the LGG Era: Harmonizing Molecular and Cytogenetic Paradigms to Support a Whole Genome Sequencing Program

Previous Eposter
726 - Using Whole Genome Sequencing to Identify Novel Variants in Branchio-Oto-Renal Syndrome

Next Eposters
733 - Update on the Online Course to Help Laboratory Professionals and Healthcare Providers Improve Preanalytic Processes of Biochemical Genetic Testing
734 - Name that panel! Variability and Clinical Validity of Commercially Available Genetic Panels for Aortic Phenotypes  
735 - MADSEQ (Mosaic Aneuploidy Detection by Sequencing) Reveals Unrecognized Chromosomal Aneuploidies in Human Samples
736 - Anticipated Positive Rates for Genetic Testing in the General Population: a “Virtual Panel” Approach
737 - Characterization of Exon Level Genomic Copy Number Changes in 1855 Normal Individuals
740 - Copy Number Variant Detection using Existing Exome and Genome Data
741 - Exome reanalysis by leveraging human phenotype ontology terms.
742 - Is microarray SNP genotyping preferred over conventional FISH/DNA tests for methylation-specific PCR positive PWS cases? Case studies and literature review
743 - Pathogenicity of Variants in ACMG Clinically Actionable Genes in the Amish
746 - Typical and Atypical Duplications within the Recurrent Xq28 int22h1/int22h2-Flanked Region to Expand Genotype-Phenotype Correlation