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Scientific News
A Cautionary Tale on Genome-Sequencing Diagnostics for Rare Diseases
Studies in several children have raising new questions about inheritance, genomic sequencing, and diagnostic.
Gene Identified Responsible for Disorders of Bones and Connective Tissue
Researchers have identified a gene that when mutated is responsible for a spectrum of disorder.
Genetic Study Shows Europeans are One Big Family
Europeans are basically one big family, closely related to one another for the past thousand years, according to a new study of the DNA of people from across the continent.
Genome Sequencing Provides Unprecedented Insight into Causes of Pneumococcal Disease
Technology will allow better surveillance of bacterial populations, understanding of vaccine effectiveness.
Tick-Borne Lone Star Virus Identified through New Super-Fast Gene Sequencing
The tick-borne Lone Star virus has been conclusively identified as part of a family of other tick-borne viruses called bunyaviruses, which often cause fever, respiratory problems and bleeding.
Launch of £90m Initiative in Big Data and Drug Discovery at Oxford University
'Big data' to revolutionise healthcare.
Why Does Smallpox Vaccine Shield Some, Not Others? It's in the Genes
How well people are protected by the smallpox vaccine depends on more than the quality of the vaccination: individual genes can alter their response, Mayo Clinic research shows.
Gifts to Boost University of Chicago as Hub for Biomedical 'Big Data'
Two major gifts will build momentum behind the University of Chicago’s leadership in biomedical computation.
AD GWAS in African Americans Confirms, Reshuffles AlzGene List
African Americans carrying a variant in a cholesterol-processing gene have double the risk for Alzheimer’s than non-carriers.
New System to Improve DNA Sequencing
A sensing system developed at Cambridge is being commercialised in the UK for use in rapid, low-cost DNA sequencing.

Genomic Analyses of Hormone Signaling and Gene Regulation
Edwin Cheung, Genome Institute of Singapore, speaking at Genomics Research Asia 2012

LATE-PCR and Its Allied Technologies maximum Information from a Single Tube Application to Mitochondria
Professor Lawrence J. Wangh, Brandeis University, speaking at Genomics Research 2012.

LATE-PCR &Thermalight Probes: Single-Tube Solutions For Personalized Cancer Medicine
Dr. J. Aquiles Sanchez, Brandeis University, speaking at Genomics Research 2012.

Single Copy qPCR-Based Detection of BRAF and KRAS Mutations
Vladimir Makarov, Swift Biosciences Inc, speaking at Genomics Research 2012.

How to Improve Interoperability of biobanks: European and International Initiatives
Kurt Zatloukal, Medical University of Graz, speaking at European Lab Automation 2012

Microfluidic Apps for Off-the-shelf Instruments
Daniel Mark, HSG-IMIT, speaking at European Lab Automation 2012

Array CGH: Applications in the Clinical Setting
Lisa D. White, Associate Professor at Baylor College of Medicine, speaking at Advances in Microarray Technology 2011.

Punctuated Evolution of Breast Tumors Revealed by Single Cell Sequencing
Dr Nicholas Navin, MD Anderson Cancer Center, speaking at Single Cell Analysis Summit 2011.

Expanding Sequencing Applications using Target Enrichment and Application to Complex Diseases Research
Dr Emily Leproust, Agilent Technologies, speaking at Next-Gen Sequencing Europe 2011.

Optimization of Multiplex Deep Sequencing Applications
Dr Leonid Bystrikh, University Medical Center Groningen, speaking at Next-Gen Sequencing Europe 2011.

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