Archived Webcasts

	Introduction to SNP & Variation Suite 7 Dr. Christophe Lambert and John Nord of Golden Helix introduce the new features and capabilities released in SNP & Variation Suite v7. ›› Access Webcast
	Genotype Calling and Imputation with BEAGLE and BEAGLECALL August 24, 2010 In this webcast, Dr. Lambert discusses the tools BEAGLECALL (to re-call genotypes) and BEAGLE (for imputation) including their advantages, limitations, when to utilize each, and comparisons to other methods. ›› Access Webcast
	Introducing SVS 7.3 July 28, 2010 The third installment of SVS 7 extends our dedication to a rich, multi-dimensional analytic approach to genetic research, empowering more people than ever to uncover the genetic cause of disease, drug response, and other conditions. ›› Access Webcast
	Achieving Genome-Wide Success Part III: Quality Assurance and Data Prep for SNP and CNV Studies December 9, 2009 The following recording is from the Golden Helix ancillary event hosted in conjunction with the 2009 American Society of Human Genetics annual meeting. Dr. Lambert examines best practices, pitfalls, and analytic methods learned from over 30 genome-wide SNP, CNV, and eQTL association studies. ›› Access Webcast
	ASHG 2009 Ancillary Event: Achieving Genome-Wide Success from SNPs to CNVs to eQTL October 22, 2009 The following recording is from the Golden Helix ancillary event hosted in conjunction with the 2009 American Society of Human Genetics annual meeting. Dr. Lambert examines best practices, pitfalls, and analytic methods learned from over 30 genome-wide SNP, CNV, and eQTL association studies. ›› Access Webcast
	Achieving Genome-Wide Success Part II: Study Design in SNP and CNV Studies October 7, 2009 Part 2 of the Achieving Genome-Wide Success, Dr. Christophe Lambert examines the effects of poor study design in genetic association studies. Strategies and techniques for good study design will also be discussed. ›› Access Webcast
	IGES 2009: Overcoming Data Quality and Copy Number Detection Issues in Genome-Wide CNV Association Studies October 19, 2009 The following is a recording of Dr. Christophe Lambert's invited talk at the International Genetic Epidemiology Society 2009 Annual Meeting. ›› Access Webcast
	Joint Statistical Meeting 2009 Talk August 5, 2009 Overcoming data quality and copy number detection issues in genome-wide CNV association studies, ›› Access Webcast
	Achieving Genome-Wide Success Part I February 18, 2009 Dr. Christophe Lambert examines some of the more persistent challenges he's experienced in SNP and CNV genome-wide association studies, and the novel methods used to overcome them. ›› Access Webcast
	Genome-Wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE December 2, 2008 Dr. Christoph Lange presents an overview of his most recent research on Alzheimer's Disease with PBAT. ›› Access Webcast
	Genome Wide SNP and CNV Association Studies Identify Genetic Factors for Lung Cancer October 28, 2008 Dr. Amos describes the approaches he and his team at The University of Texas have taken in identifying genetic factors influencing the risk for lung cancer development. ›› Access Webcast
	IGES 2008 Talk: Methods and Discoveries Drawn from 20 Whole Genome Copy Number Variation Studies September 16, 2008 Includes discussion of Wellcome Trust copy number variation association results. ›› Access Webcast
	Emerging Methods in Whole Genome CNV Association July 23, 2008 Discussion of key strategies, methods and workflows used on over twenty whole genome copy number variation (CNV) association studies. ›› Access Webcast
	On the Analysis of Copy-Number Variations in Genome-Wide Association Studies: A Translation of the Family-Based Association Test March 18, 2008 Dr. Christoph Lange presents an overview of his recent work with Dr. Juliana Ionita-Laza on analyzing copy number variations in family-based association studies using PBAT. ›› Access Webcast
	On the Replication of Genetic Associations: Timing Can Be Everything April 15, 2008 Dr. Jessica Lasky Su presents discusses her research and the PBAT methods used to find a whole genome age-dependent association that was replicated in five of eight studies. ›› Access Webcast
	SNP, ROH and CNV Association Analysis Overview with Affymetrix SNP Arrays 5.0 and 6.0 February 7, 2008 An overview of various whole genome methods and workflows for analyzing Affymetrix SNP and copy number data with the SNP & Variation Suite. ›› Access Webcast
	Whole Genome Copy Number Association Analysis with Golden Helix November 14, 2007 A first look at the CNV segmentation and association methods implemented in the Copy Number Analysis Module (CNAM). ›› Access Webcast
	Using Runs of Homozygosity to Identify Recessive Loci January 24, 2008 Dr. Todd Lencz address the theoretical and statistical underpinnings of whole genome homozygosity association (WGHA) and its potential utility in studies of complex disease. ›› Access Webcast
	Whole Genome Association Study of Schizophrenia May 9, 2007 Dr. Todd Lencz presents the analysis and results of his whole genome association study of Schizophrenia. ›› Access Webcast

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Archived Webcasts