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Applications of Next-Generation Sequencing in Clinical Care
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Rick Dewey, MD
Stanford Center for Inherited Cardiovascular Disease
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Wednesday, December 7, 2011
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Learn how the GenoLogics LIMS significantly improved operations at an Illumina FastTrack Sequencing Services lab in a few weeks
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Melissa Kamkar
Applications Scientist - Team Lead,
GenoLogics
Christian Haudenschild
Vice President of Product Development,
Illumina
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Thursday, December 1st, 2011
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TruSeq Custom Amplicon: Learn How to Customize Content with DesignStudio
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Layla Katiraee, Ph.D.
Senior Scientist,
New Product Transfer
Jonathan Bell
Product Manager,
DNA Sequencing Applications
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Thursday, November 17, 2011
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Optimization of Illumina mRNA-Seq and Conversion to a User-Friendly Analysis Solution
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Dr. Joel Parker
Principal Scientist,
Expression Analysis
Gabe Rudy
Vice President of Product Development,
Golden Helix
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Thursday, November 3, 2011
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Using IPA® to analyze Illumina RNA-Seq data reveals abundance-specific biological signatures in Alzheimer's Disease
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Darryl Gietzen, Ph.D.
Field Application Scientist,
Ingenuity Systems
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Monday, October 10, 2011
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TruSeq Custom Enrichment: Learn How to Customize Content with DesignStudio
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Scott O'Brien
Sr. Product Manager,
DNA Sequencing Applications
John Izzo, Ph.D.
Sr. Scientist
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Thursday, September 1, 2011
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Moving Forward on a Framework for Analysis of Diagnostic and Incidental Results of Whole Exome / Genome Sequencing
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Jonathan S. Berg, MD, PhD
Assistant Professor, Department of Genetics
Member, Lineberger Comprehensive Cancer Center
Associate Director, Carolina Center for Genome Sciences
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Thursday, July 28, 2011
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Optimized Alignment and Variant calling using Illumina’s CASAVA 1.8 Software
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Eric E. Smith, Ph.D.
Bioinformatics Scientist, Illumina
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Tuesday, June 21, 2011
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Introduction to RNA Sequencing Data Analysis
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Amy Bouck-Knight, Ph.D.
Bioinformatics Support Scientist, Illumina Technical Support
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Thursday, May 26, 2011
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The ClinSeq Project: An Approach to Clinical Genomics Research.
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Leslie G. Biesecker, M.D.
Sr. Investigator and Head, Human Development Section,
Laboratory of Genetic Disease Research, NHGRI, NIH
Flavia M. Facio, M.S., CGC
Genetic Counselor,
Genetic Disease Research Branch, NHGRI, NIH
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Tuesday, May 10, 2011
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CASAVA 1.8, what is new!
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Lukas Smink, Ph.D.
Product Marketing Manager, Sequencing & Informatics - EMEA, Illumina
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Monday, May 9, 2011
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My Sample. My Study. MiSeq. Introducing Illumina's personal sequencing system.
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Rob Tarbox
Sr. Product Manager
Illumina
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Wednesday, April 20, 2011
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Next Generation Sequencing Software Presentation by Data2Bio
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Patrick Schnable, Ph.D.
Director
Center for Plant Genomics, Iowa State University
Managing Partner Data2Bio
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Friday, April 1, 2011
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TruSeq Exome Enrichment: The Technology Behind the Latest Targeted Resequencing Solution
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David Williamson, Ph.D.
Bioinformatics Scientist 2
Illumina
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Thursday, March 24, 2011
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Eco Software Version 3.0 Training
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Illumina Technical Support Team
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Tuesday, March 1, 2011
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Introducing the NEW Infinium HD FFPE Sample Solution
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Alex Helm
Product Manager
Illumina
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Wednesday, January 19, 2011
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Exome Sequencing & Mendelian Genetics
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Jay Shendure, MD, Ph.D.
Assistant Professor
Department of Genome Sciences, University of Washington
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Wednesday, December 15, 2010
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Mining the Cancer Methylome
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Peter W. Laird, Ph.D.
Director
USC Epigenome Center
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Wednesday, December 8, 2010
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TruSeq Data Quality and Accuracy
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Dipesh Risal, Ph.D.
Senior Product Manager
Informatics, Illumina, Inc.
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Thurs, November 18, 2010
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RNA Sequencing vs. Arrays: Superior Data at a Lower Cost than Arrays
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Shawn Levy, Ph.D.
Faculty Investigator
Hudson Alpha Institute for Biotechnology
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Tuesday, November 16, 2010
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Refining Cardiovascular and Metabolic Genetic Associations using Custom Arrays
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Benjamin F. Voight, Ph.D.
Research Scientist, Medical Population Genetics
The Broad Institute of Harvard and MIT
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Wed, November 10, 2010
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Eco Real-Time PCR System Virtual Demonstration Webinar
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Russell Nofsinger, PhD.
Field Application Scientist
Sandrine Miller, Pharm.D., Ph.D.
Senior Product Manager, PCR
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Tue, November 09, 2010
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RNA Sequencing: Straightforward Data Analysis
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Cole Trapnell
Postdoctoral Research fellow, Harvard Medical School and the Broad Institute of MIT and Harvard
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Tue, October 26, 2010
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Illumina Genome Network: Whole Genome Sequencing Services Without Compromise.
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Tanya Boyaniwsky
Senior Market Manager, Illumina
Jordan Stockton, Ph.D.,
Senior Market Manager, Computational Biology, Illumina
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Wed, October 20, 2010
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RNA Sequencing: The Right Choice for Any Lab
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Christopher E. Mason, Ph.D.,
Assistant Professor, Weill Medical College of Cornell University
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Tue, October 5, 2010
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Next-gen GWAS. The Scientist Behind SNP Selection
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Dr. Mike Eberle,
Senior Staff Bioinformatics Scientist, Illumina
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Wed, September 29, 2010
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The Continuum of Bovine Genomic Innovation
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Andre Eggen, Ph.D,
Agrigenomics Sales Specialist, Illumina
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Wed, July 21, 2010
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An Overview of Novel Nucleic Acid Stabilization Technologies
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Dr Rolf Muller,
Founder, President & CSO, Biomatrica Inc.
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Wed, June 2, 2010
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An Illumina-Demonstrated Method for Sequencing the Complete Transcriptome
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Gary Schroth, Ph.D.,
Sr. Director, Gene Expression Applications R&D, Illumina
Shujun Luo,
Sr. Staff Scientist, Illumina
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Wed, May 5, 2010
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Designing Allele Specific Primer Extension Assays with the VeraCode Assay Designer
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Tera Eerkes, Ph.D.,
Chief Scientific Officer, iGenix, Inc.
Raymond J. Peterson, Ph.D.,
Chief Scientific Officer, Celadon Laboratories
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Tue, Apr. 6, 2010
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Next-Gen Sequencing Made Accessible: How the Genome Analyzer IIe Can Benefit Your Research
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Rob Tarbox
Illumina
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Wed, Mar. 17, 2010
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Next-Generation Genotyping Studies: Bringing the Power of Recent Discoveries to Your Research
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Jennifer Stone, Ph.D.
Illumina
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Wed, Feb. 3, 2010
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Advances in Next-Generation Sequencing – Moving Basic Research into the Clinical Lab
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Mark Ross, Ph.D.
Illumina
Tina Hambuch, Ph.D.
Illumina
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Wed, Jan. 20, 2010
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How USC Leverages Bioinformatics Technologies For Epigenomics Research
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Dr. Benjamin Berman
Sr. Research Associate - Bioinformatics, USC Epigenome Center
Mike Sanders
Genomics Product Manager, GenoLogics Life Sciences Software
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Tue, Dec. 15, 2009
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Genome-wide Translational Profiling by Deep Sequencing of Ribosome Footprints
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Nicholas T. Ingolia, Ph.D.
Postdoctoral fellow, Weissman Laboratory
University of California, San Francisco
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Wed, Dec. 9, 2009
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Advanced Technology for Storage and Transport of Nucleic Acids for use in Genetic Analysis
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Heather Martinez, Ph.D.
Applications Support Manager, GenVault
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Wed, Dec. 2, 2009
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Finding the Fifth Base: Human DNA Methylomes at Single-base Resolution Show Widespread Epigenomic Differences
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Ryan Lister, Ph.D.
The Salk Institute for Biological Studies, Joe Ecker's Lab
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Wed, Nov. 18, 2009
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Introduction to the VeraCode ADME Core Panel for multiplexed Genotyping of Pharmacogenetic Biomarkers
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Naomi O'Grady,
Product Manager, Molecular Diagnostics, Genotyping
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Wed, Oct. 28, 2009
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Copy Number Detection at a Cytogenetic Level
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Ing. Bert Eussen,
Department of Clinical Genetics, Erasmus MC
Dr. A. de Klein,
Department of Clinical Genetics, Erasmus MC
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Wed, Sep. 30, 2009
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Copy Number Variation at 1q21.1 Associated with Neuroblastoma: A Review of Recent CNV Work from the Maris/Hakonarson Labs
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Sharon Diskin, Ph.D.,
Center for Applied Genomics, The Children’s Hospital of Philadelphia
Hakon Hakonarson, M.D., Ph.D.,
Center for Applied Genomics, The Children’s Hospital of Philadelphia
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Wed, August 26, 2009
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Chimera Transcript Discovery Using Next Generation Transcriptome Sequencing
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Christopher Maher, Ph.D., Research Fellow,
Chinnaiyan Lab, Michigan Center for Translational Pathology
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Wed, Aug 19, 2009
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Customized Strategies for Targeted Genotyping, Expression and Methylation Studies in Human, Mitochondrial, and Non-Human Genomes
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Tera Eerkes, Ph.D., CEO,
iGenix, Inc.
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Wed, Aug 5, 2009
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SNP Arrays Open a Window on Complex Mosaicism
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Laura Conlin, Ph.D.
Children's Hospital of Philadelphia
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Wed, Jul. 8, 2009
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GoldenGate Indexing: A New Evolution in High-Throughput Screening
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Jason Downing,
Product Manager, GoldenGate Genotyping, Illumina
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Wed, Jul. 15, 2009
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Analysis of mRNA-Seq Data in Partek Genomics Suite
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Michael Lelivelt,
Vice-President, Genomics Partek
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Wed, May 27, 2009
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End-to-End Workflow Management for the Illumina Genome Analyzer
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Mike Sanders,
Product Manager, GenoLogics
Mark Luszniak,
Field Applications Specialist, GenoLogics
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Wed, May 20, 2009
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Comprehensive, Fast, and User-Friendly Downstream Analysis of Illumina Sequencing Data
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Dr. Roald Forsberg Ph.D.,
Bioinformatics and Director of Scientific Software Solutions, CLC bio
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Wed, Feb. 18, 2009
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Array Differences in Genomic Coverage and Data Quality Impact on GWAS Success
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David L. Delano, Ph.D.,
Scientific Affairs, Illumina
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Wed, Nov. 19, 2008
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Using mRNA-Seq to Explore Agricultural Transcriptomics
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Dr. Gregory May, Ph.D.,
Director, Genome Sequencing Center National Center for Genome Resources
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Wed, Oct. 29, 2008
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Genotyping Complex Polymorphic Regions with the VeraCode® Assay Designer for Low Multiplex Panels
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Daniel LaFlamme, Ph.D.,
Laboratory Manager, Sciona
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Wed, Oct. 22, 2008
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Mapping and Quantifying Mammalian Transcriptomes by RNA-Seq on the Illumina Genome Analyzer
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Ali Mortazavi, Ph.D.,
Postdoctoral Fellow California Institute of Technology Barbara Wold Lab
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Fri, Sep. 12, 2008
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Integrated Molecular Portraits of Platinum Resistance in Ovarian Cancer
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John Quackenbush, Ph.D.,
Dana-Farber Cancer Institute
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Wed, Aug. 6, 2008
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Mapping the Arabidopsis Epigenome and Transcriptome by Deep Sequencing
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Ryan Lister, Ph.D.,
The Salk Institute for Biological Studies - Joe Ecker Lab
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Wed, Jul. 16, 2008
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Illumina-ting the Origins of the Domestic Cat – Efficiency of the GoldenGate® Assay for VeraCode® in Cat Genetics
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Leslie A. Lyons, Ph.D.,
Associate Professor, Dept. of Population Health & Reproduction, School of Veterinary Medicine, University of California, Davis
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Wed, Jul. 9, 2008
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Sequencing an Individual African Human Genome
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David R. Bentley, Ph.D.,
Vice President and Chief Scientist, Illumina
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Tue, Jun. 24, 2008
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GoldenGate and Infinium SNP Genotyping for Association Studies in Trees
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David B. Neale, Ph.D.,
Professor, Department of Plant Sciences, University of California, Davis
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Mon, Jun. 23, 2008
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Genome-Wide Association Scan in Women with Systemic Lupus Erythematosus Identifies Susceptibility Variants in ITGAM, PXK, KIAA1542 and other Loci
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Robert P. Kimberly, MD,
UAB Arthritis and Musculoskeletal Center/University of Alabama at Birmingham
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Thu, May 8, 2008
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From Sample to Results: Managing Illumina® Sequencing Data Workflow with FinchLab
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Todd Smith, Ph.D.,
Geospiza, Inc.
|
Wed, Apr. 23, 2008
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Analysis of Copy Number Variation in Genome-Wide Association Studies: A Family-Based Approach
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Iuliana Ionita-Laza, Ph.D.,
Postdoctoral Fellow, Harvard School of Public Health
Christoph Lange, Ph.D.,
Associate Professor, Harvard Medical School
|
Fri, Apr. 4, 2008
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Population Genomics of Human Gene Expression
|
Emmanouil T. Dermitzakis, Ph.D.,
Investigator, Population and Comparative Genomics
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus
|
Wed, Mar. 5, 2008
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Human Genome Sequencing
|
David R. Bentley, Ph.D.,
Vice President and Chief Scientist, Illumina
|
Wed, Feb. 13, 2008
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DASL® Gene Expression on the VeraCode® Platform to Study Alternative Splicing
|
Brenton R. Graveley, Ph.D.,
Associate Professor of Genetics and Developmental Biology
University of Connecticut Health Center
|
Wed, Jan. 23, 2008
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Get the Power you Need with Illumina's DNA Analysis Products
|
Carsten Rosenow, Ph.D.,
Senior Market Manager, DNA Analysis Products, Illumina
Omoshile Clement, Ph.D.,
Senior Product Manager, Systems, Illumina
|
Tue, Oct. 30, 2007
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ChIP-Seq: Global Measurement of Occupancy of DNA Binding Proteins by Sequence Counting
|
David Johnson, Ph.D.,
Senior Scientist, Department of Genetics, Stanford University
Ali Mortazavi,
Division of Biology, California Institute of Technology
|
Thu, Jun. 21, 2007
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High-throughput DNA Methylation Profiling
|
Dr. Peter W. Laird
|
Mon, Feb. 12, 2007
|
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A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene
|
Dr. Richard H. Duerr
Dr. Judy H. Cho
|
Mon, Jan. 15, 2007
|
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High-resolution Genomic Profiling of Chromosomal Aberrations Using Infinium® Whole Genome Genotyping
|
Daniel Peiffer Ph.D.,
Illumina, Inc.
|
Tue, Nov. 28, 2006
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Capturing Common Multi-Ethnic Human Variation on a Single Microarray
|
Dr. Sarah Shaw Murray,
Illumina, Inc.
|
Mon, Oct. 30, 2006
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