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Scientific News
Whole-Genome Sequencing Successfully Identifies Cancer-Related Mutations
UT Southwestern Medical Center cancer researchers have demonstrated that whole-genome sequencing can be used to identify patients’ risk for hereditary cancer.
NHS Genomic Medicine Centres Announced for 100,000 Genomes Project
Eleven centres have been announced across England, to lead the way in delivering the 100,000 Genomes Project.
Promising Compound Rapidly Eliminates Malaria Parasite
An international research collaborative led by St. Jude Children’s Research Hospital reports that the rapid action of (+)-SJ733 will likely slow malaria drug resistance.
Genes that Cause Pancreatic Cancer Identified by New Tool
Screening system in mice spots cancerous changes invisible to sequencing.
Using Genome Sequencing to Track MRSA in Under-resourced Hospitals
Whole genome sequencing of MRSA from a hospital in Asia has demonstrated patterns of transmission in a resource-limited setting, where formal screening procedures are not feasible.
Comprehensive Genomic Study of Sub-Saharan Africans Conducted
New data resource will enhance disease research and genomic diversity studies.
Genetic Errors Linked to More ALS Cases than Scientists had Thought
Number of mutated genes influences the age when the fatal paralyzing disorder first appears.
WormBase ParaSite Launched
Open-access database WormBase ParaSite launches with data on 1.5 million genes.
Big Data Set To Make A Big Difference In Childhood Cancer Treatment
UTS researchers are working with the Kids Research Institute to visualise large quantities of patient data to better diagnose and treat childhood cancer patients.
Two Studies Identify A Detectable, Pre-Cancerous State In The Blood
Findings pave way for new lines of cancer research focused on detection and prevention.

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.

Cancer Methylome Profiling using Methyl-DNA Capture
Dr Arjen Brinkman, Radboud University Nijmegen (NL), speaking at Next-Gen Sequencing Europe 2011.

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