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Sample Prep Conference - Day 2




Day 1 | Day 2 | Download Brochure  

Thursday, April 11

8:00-8:55am Breakout Discussions and Morning Coffee


Topics To Be Discussed:

Nanotechnology Applications in Molecular Diagnostics
Moderator: Martin Hegner, Ph.D., Professor, Centre for Research on Adaptive Nanostructures and Nanodevices, Trinity College Dublin, Ireland

Sample Prep for Molecular Diagnostics of Infectious Diseases
Moderator: Martin Siaw, Ph.D., Staff Scientist and Associate Director, Advanced Sequencing Core, Advanced Sequencing, Quest Diagnostics Nichols Institute

Nucleic Acid Extraction
Moderator: Corey Braastad, Ph.D., Scientific Director, Athena Diagnostics

Working with FFPE Samples
Moderator: Sandra M. Gaston, Ph.D., Director, Molecular Biomarkers Research Laboratory, Department of Pathology and Laboratory Medicine, Tufts Medical Center Assistant Professor of Pathology, Tufts University School of Medicine

 

Nanotechnology for IVD Sample Prep 

8:55-9:00 Chairperson's Remarks
Martin Siaw, Ph.D., Staff Scientist and Associate Director, Advanced Sequencing Core, Advanced Sequencing, Quest Diagnostics Nichols Institute

9:00-9:30 Quantitative Nanomechanical Diagnostics – Direct Label Free Noncoding RNA Detection from Serum

Martin Hegner, Ph.D., Professor, Centre for Research on Adaptive Nanostructures and Nanodevices, Trinity College Dublin, Ireland

Ultra sensitive nanomechanical sensing platforms for label-free qualitative and quantitative bio-analytical measurements will change the way we perform diagnostics.  We demonstrate that cantilever array sensors are capable to directly track the pharmacokinetics of therapeutic siRNA molecules in tissues and the early detection of miRNA biomarker molecules, which indicate organ pathology induced by adverse drug effects measured from blood serum. 

9:30-10:00 Nanofiber-Based Sample Preparation for Diagnostic Devices

Antje Baeumner, Ph.D., Professor, Biological and Environmental Engineering, Cornell University

We investigate the use of electrospun nanofibers as highly effective material for the selective enrichment of analytes from samples. We have demonstrated the reliable fabrication of nanofiber mats embedded in microfluidic channels. We have also demonstrated selective capture and release of nanoparticles and bacterial cells. We have further shown that nanofiber mats can function as effective passive microfluidic mixer. Applications for complex microTAS and simple Point-of-Care devices are targeted.

10:00-10:30 Sponsored Presentations (Opportunities Available)

10:30-11:00 Coffee Break with Exhibit and Poster Viewing

 

Sample Prep Considerations in Pathogen Detection 

11:00-11:30 Sample Preparation for Molecular Diagnostics in a CLIA Certified Clinical Laboratory: Nucleic Acid Extraction and Target Enrichment for Pathogen Testing by Next-Generation Sequencing

Martin Siaw, Ph.D., Staff Scientist and Associate Director, Advanced Sequencing Core, Advanced Sequencing, Quest Diagnostics Nichols Institute

Sample preparation is an important component of any molecular testing that is being done in clinical laboratories. Improvements in nucleic acid extraction and target enrichment are considered to be critical to the workflow of diagnostic tests involving the use of NGS. My presentation will focus on the requirements for CLIA certified clinical laboratories, the various patient specimens to be tested, the methods currently in use for nucleic acid extraction and target enrichment and the commercial kits available in the market. The focus will be on pathogen testing by NGS.

11:30-12:00 pm Direct Selection of Microbiome DNA from Human DNA

Erbay Yigit, Scientist, Applications and Product Development, New England Biolabs

Microbiome is an integral part of human life, and perturbations in microbiome-host balance can lead to human disease. Recently, next generation sequencing technologies have enabled the analysis of the human microbiome. However, the analysis of a microbiome can be both monetarily and computationally expensive, due to the contamination of host DNA in a sample, requiring deep sequencing to be able to detect some microbial species. To overcome this problem, we developed a microbiome enrichment kit that reduces host DNA contamination nearly 50-fold, corresponding to ~90-95% microbiome DNA in the enriched fraction. This simple methodology can be used to analyze entire microbiomes in a cost-effective manner utilizing established next generation sequencing platforms, as well as newer single molecule sequencing technologies.

12:00 Close of Conference


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