ASHG 2018 CoLab Schedule CoLab #1 Booth #1441 DATA CLINICAL LABORATORY OTHER NO COLAB

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1 ASHG 2018 CoLab Schedule CoLab #1 Booth #1441 DATA CLINICAL LABORATORY OTHER NO COLAB Wed. Sponsor Topic Thursday Sponsor Topic Friday Sponsor Topic 10:00 am 10:30 am Covaris Standardization of the ChIP Workflow Using Covaris Adaptive Focused Acoustics (AFA) to Study the Transcriptional Regulation of SOD1 in ALS Pathogenesis 10:30 am 11:00 am Color Genomics Color Data: an Aggregated Genotypicphenotypic Database of 50,000 Individuals for Hereditary Cancer Risk 10:00 am 10:30 am Enancio Lena for a Powerful Compression of Your Genomics Data Golden Helix Streamlining ACMG Variant Interpretation Guidelines Shire Medical Affairs Clinical and Scientific Advances in Lysosomal Storage Disorders (LSDs) WuXi NextCODE Different Approaches to Immuno oncology Analysis of Somatic Samples and Different Answers TMB, MSI, and More 1:45 pm 2:15 pm Clear Genetics Artificial Intelligence and Chatbots To Scale the Delivery of Genomic Medicine 1:45 pm 2:15 pm Rady Children's Institute for Genomic Medicine Rapid Whole Genome Sequencing for Guiding Treatment in Neonatal and Pediatric Intensive Care Units 1:45 pm 2:00 pm 2:30 pm 3:00 pm DNA Genotek How to Provide the Most Appealing Path to Attract Research Participants 2:30 pm 3:00 pm Golden Helix Fine tuning CNV Analysis for the Clinical Analysis of NGS Samples 2:30 pm 3:00 pm AJHG AJHG Author Update: Massively Parallel Functional Genomics with Jay Shendure 3:15 pm 3:45 pm Fabric Genomics Joint Clinical Interpretation of Structural and Small Variants in Whole Genomes for the Diagnosis of Genetic Disorders 3:15 pm 3:45 pm ASHG Trainee Lighting Talks on Complex Traits, Genomics, and more: Highlights from Trainee Paper Spotlight 3:15 pm 3:45 pm Roche Sequencing and Life Science Enabling NGS based CRISPR QC Applications with Robust, Highperformance DNA Library Preparation Workflows 4:00 pm 4:30 pm Roche Sequencing and Life Science Robust Library Preparation for Improved Ultra low Input and Flexible Single cell RNAsequencing 4:00 pm 4:30 pm Human Longevity AI driven Risk Prediction for Chronic Age related Disease from Genomic, Imaging and Clinical Biomarkers 4:00 pm 4:30 pm

2 ASHG 2018 CoLab Schedule CoLab #2 Booth #1005 DATA CLINICAL LABORATORY OTHER NO COLAB 10:00 am 10:30 am Ilumina What s New from Illumina: Enabling Novel Approaches to NGS based Research 10:30 am 11:00 am NIH/NCBI NCBI Pharmacogenetics Resources for Clinical Care 10:00 am 10:30 am Brand Buddha Future of Client Acquisition & Adherence Microsoft Empower Health with Microsoft Genomics WuXi NextCODE Demonstrating the WuXi NextCODE Suite of Tools to do Deep Phenotypic and Genomic Analysis on Half a Million Patients Ambry Genetics Maximizing Genetic Testing for Hereditary Cancer Using RNA Sequencing 1:45 pm 2:15 pm Sophia Genetics Democratizing Data Driven Medicine 1:45 pm 2:15 pm MediSapiens Ltd Real Time Querying of 500 K Genomes and Clinical Data in the Cloud 1:45 pm 2:15 pm Beckman Coulter Number of Fusions Detected in FFPE Cancer Tissue Depends on RNA Isolation Method 2:30 pm 3:00 pm Sophia Genetics Democratizing Data Driven Medicine, continue 2:30 pm 3:00 pm elife How to Publish your Best Work with elife 2:30 pm 3:00 pm Databricks Accelerating Genomic Data Processing and Tertiary Analytics at Biobank scale 3:15 pm 3:45 pm Genomenon Impact Study Results: Reconciling Inconsistency Among commercial NGS Gene Panels via an Evidencebased Curation Platform 3:15 pm 3:45 pm Lipotype GmbH Combining Genomics with Shotgun Lipidomics the Power of Multi omics Approaches 3:15 pm 3:45 pm 4:00 pm 4:30 pm Google Cloud Omics Big Data and Analytics at Google Cloud 4:00 pm 4:30 pm DNASTAR Inc. Large Scale Variant Analysis: The Challenge of Turning Big Data into Meaningful Results 4:00 pm 4:30 pm

3 ASHG 2018 CoLab Schedule CoLab #3 Booth #241 DATA CLINICAL LABORATORY OTHER NO COLAB 10:00 am 10:30 am Agilent Technologies The QUICK Analysis: Quickly Uncovering Important Clinical Knowledge in the Diagnostic Setting 10:30 am 11:00 am 10x Genomics Accelerating Biology: New Product Innovations from 10x Genomics 10:00 am 10:30 am PacBio Solving Human Diseases with PacBio Sequencing of Structural Variants and Alternative Splicing PerkinElmer Genomics From Newborn Screening to Whole Genome Sequencing Innovation Driven through Technology and Clinical Expertise Agilent Technologies CanPathPro Development of a Platform for Predictive Cancer Pathway Modelling using Genetically Engineered Mouse Models Synthego How to Empower your Research with CRISPR 1:45 pm 2:15 pm Dovetail Genomics Structural Variation Detection by Proximity Litagation from FFPE Tumor Tissue 1:45 pm 2:15 pm 10x Genomics Unraveling Multiple Dimensions of Cellular Heterogeneity 1:45 pm 2:15 pm 10x Genomics Visualization of Multiple Single Cell Genomic Datatypes 2:30 pm 3:00 pm NIH/NCBI Interactive Visualization of NCBI Annotations for Variant Interpretation 2:30 pm 3:00 pm Quantabio New Q qpcr Cycler Redefines Runtime to as Little as 25 minutes While Enhancing Performance for Molecular Testing Applications 2:30 pm 3:00 pm ASHG Early Career Conversations: Successes and Challenges of Junior Faculty Positions 3:15 pm 3:45 pm Promega Ask the Expert Session: Nucleic Acid Extraction, Analysis Strategies and Pitfalls 3:15 pm 3:45 pm Agilent Technologies A Guide in the Darkness: Assessing the Quality of Chemically Synthesized RNAs used in CRISPRbased Genome Engineering 3:15 pm 3:45 pm ASHG Early Career Conversations: Successes and Challenges of Junior Faculty Positions, continue 4:00 pm 4:30 pm 10x Genomics Getting Started with Single Cell Transcriptomics 4:00 pm 4:30 pm Petagene Using Data Compression to Address the Challenges of Ever Increasing Volumes of Genomics Data 4:00 pm 4:30 pm

4 CoLab Theater 1 Booth #1441 Wednesday, October 17, :30pm 3:00pm 3:15pm 3:45pm 4:00pm 4:30pm Title: Standardization of the ChIP Workflow Using Covaris Adaptive Focused Acoustics (AFA)to Study the Transcriptional Regulation of SOD1 in ALS Pathogenesis Presented by: Covaris Title: Streamlining ACMG Variant Interpretation Guidelines Presented by: Golden Helix Title: Artificial Intelligence and Chatbots To Scale the Delivery of Genomic Medicine Presented by: Clear Genetics Title: How to Provide the Most Appealing Path to Attract Research Participants Presented by: DNA Genotek Title: Joint Clinical Interpretation of Structural and Small Variants in Whole Genomes for the Diagnosis of Genetic Disorders Presented by: Fabric Genomics Title: Robust Library Preparation for Improved Ultra low Input and Flexible Single cell RNA sequencing Presented by: Roche Sequencing and Life Sciences Thursday, October 18, :30am 11:00am Title: Color Data: An Aggregated Genotypic phenotypic Database of 50,000 Individuals for Hereditary Cancer Risk Presented by: Color Genomics Title: Clinical and Scientific Advances in Lysosomal Storage Disorders (LSDs) Presented by: Shire Medical Affairs 2:30pm 3:00pm Title: Rapid Whole Genome Sequencing for Guiding Treatment in Neonatal and Pediatric Intensive Care Units Presented by: Rady Children's Institute for Genomic Medicine Title: Fine tuning CNV Analysis for the Clinical Analysis of NGS Samples Presented by: Golden Helix

5 3:15pm 3:45pm 4:00pm 4:30pm Title: Trainee Lighting Talks on Complex Traits, Genomics, and more: Highlights from Trainee Paper Spotlight Presented by: American Society of Human Genetics Title: AI driven risk Prediction for Chronic age related Disease from Genomic, Imaging and Clinical Biomarkers Presented by: Human Longevity Friday, October 19, :15pm 3:00pm 3:15pm 3:45pm Title: Lena for a Powerful Compression of Your Genomics Data Presented by: Enancio Title: Different Approaches to Immuno oncology Analysis of Somatic Samples and Different Answers TMB, MSI, and More Presented by: WuXi NextCODE Title: AJHG Author Update: Massively Parallel Functional Genomics with Jay Shendure Presented by: American Journal of Human Genetics Title: Enabling NGS based CRISPR QC Applications with Robust, Highperformance DNA Library Preparation Workflows Presented by: Roche Sequencing and Life Sciences

6 CoLab Theater 2 Booth #1005 Wednesday, October 17, :30pm 3:00pm 3:15pm 3:45pm 4:00pm 4:30pm Title: What s New from Illumina: Enabling Novel Approaches to NGS based Research Presented by: Illumina Title: Empower Health with Microsoft Genomics Presented by: Microsoft Title: Democratizing Data Driven Medicine Presented by: Sophia Genetics Title: Democratizing Data Driven Medicine, continued Presented by: Sophia Genetics Title: Impact Study Results: Reconciling Inconsistency Among Commercial NGS Gene Panels via an Evidence based Curation Platform Presented by: Genomenon Title: Omics Big Data and Analytics at Google Cloud Presented by: Google Cloud Thursday, October 18, :30am 11:00am 2:30pm 3:00pm 3:15pm 3:45pm Title: NCBI Pharmacogenetics Resources for Clinical Care Presented by: NIH/NCBI Title: Demonstrating the WuXi NextCODE Suite of Tools to do Deep Phenotypic and Genomic Analysis on Half a Million Patients Presented by: WuXi NextCODE Title: Real Time Querying of 500K Genomes and Clinical Data in the Cloud Presented by: MediSapiens Ltd Title: How to Publish your Best Work with elife Presented by: elife Title: Combining Genomics with Shotgun Lipidomics the Power of Multi omics Approaches Presented by: Lipotype GmbH

7 4:00pm 4:30pm Title: Large Scale Variant Analysis: The Challenge of Turning Big Data into Meaningful Results Presented by: DNASTAR Inc. Friday, October 19, 2018 Title: Future of Client Acquisition & Adherence Presented by: Brand Buddha Title: Maximizing Genetic Testing for Hereditary Cancer Using RNA Sequencing Presented by: Ambry Genetics Title: Number of Fusions Detected in FFPE Cancer Tissue Depends on RNA Isolation Method Presented by: Beckman Coulter 2:30pm 3:00pm Title: Accelerating Genomic Data Processing and Tertiary Analytics at Biobank scale Presented by: Databricks

8 CoLab Theater 3 Booth #241 Wednesday, October 17, :30pm 3:00pm 3:15pm 3:45pm 4:00pm 4:30pm Title: The QUICK Analysis: Quickly Uncovering Important Clinical Knowledge in the Diagnostic Setting Presented by: Agilent Technologies Title: From Newborn Screening to Whole Genome Sequencing Innovation Driven through Technology and Clinical Expertise Presented by: PerkinElmer Genomics Title: Structural Variation Detection by Proximity Ligation from FFPE Tumor Tissue Presented by: Dovetail Genomics Title: Interactive Visualization of NCBI Annotations for Variant Interpretation Presented by: NIH/NCBI Title: Ask the Expert Session: Nucleic Acid Extraction, Analysis Strategies and Pitfalls Presented by: Promega Title: Getting Started with Single Cell Transcriptomics Presented by: 10x Genomics Thursday, October 18, :30am 11:00am Title: Accelerating Biology: New Product Innovations from 10x Genomics Presented by: 10x Genomics 2:30pm 3:00pm Title: CanPathPro Development of a Platform for Predictive Cancer Pathway Modelling using Genetically Engineered Mouse Models Presented by: Agilent Technologies Title: Unraveling Multiple Dimensions of Cellular Heterogeneity Presented by: 10x Genomics Title: New Q qpcr Cycler Redefines Runtime to as Little as 25 minutes While Enhancing Performance for Molecular Testing Applications Presented by: Quantabio

9 3:15pm 3:45pm 4:00pm 4:30pm Title: A Guide in the Darkness: Assessing the Quality of Chemically Synthesized RNAs used in CRISPR based Genome Engineering Presented by: Agilent Technologies Title: Using Data Compression to Address the Challenges of Ever Increasing Volumes of Genomics Data Presented by: PetaGene Friday, October 19, :45pm 1:30pm 2:30pm 3:45pm Title: Solving Human Diseases with PacBio Sequencing of Structural Variants and Alternative Splicing Presented by: PacBio Title: How to Empower Your Research with CRISPR Presentation: Synthego Title: Visualization of Multiple Single Cell Genomic Datatypes Presented by: 10x Genomics Title: Early Career Conversations: Successes and Challenges of Junior Faculty Positions Presented by: American Society of Human Genetics