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  Events - October 2012


Next Generation Sequencing Asia Congress

01 Oct 2012 - 02 Oct 2012 - Singapore



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Over 200 NGS, Genomics, Metagenomics, Epigenetics, Bioinformatics & Data Management senior scientists from Asia

Over 60 outstanding case studies and presentations

5 conference streams including:-

•    Next Generation Sequencing Technologies
•    Innovations in Epigenetics, Analytical Genomics & Copy Number Variation
•    NGS Application Case Studies
•    NGS Application Case Studies in Oncology
•    Data Analysis, Storage & Management

The 2nd Annual Next Generation Sequencing Asia Congress is to be held on the 1st and 2nd of October in Singapore. Over the 2 days, the conference will provide an overview of the current options of next-generation sequencing platforms, technologies, applications and the newest computational tools for the analysis of next-generation sequencing data and analytical genomics as well as overcoming data management problems.

The event will attract over 200 senior-level decision makers working in areas such as next generation sequencing, analytical genomics, computational biology, oncology, RNA profiling, molecular genomics, biomarkers, bioinformatics & data management and clinical & diagnostics development from countries such as China, Japan, Singapore, Australia, Taiwan, S.Korea, Hong Kong & surrounding countries.

This prestigious event provides a forum for practitioners and researchers to learn more about key solutions being provided to their industry, analysis of current technologies, network with their peers and address key industry concerns through a series of cutting edge conference presentations in a professional yet relaxed environment.



Further information
Scientific News
Advancing Protein Visualization
Cryo-EM methods can determine structures of small proteins bound to potential drug candidates.
Gene Expression Controls Revealed
Researchers have modelled every atom in a key part of the process for switching on genes, revealing a whole new area for potential drug targets.
Making Genetic Data Easier to Search
Scripps team streamlines biomedical research by making genetic data easier to search.
Monovar Drills Down Into Cancer Genome
Rice, MD Anderson develop program to ID mutations in single cancer cells.
It’s Now Easier To Go With The Flow
Rice University tool simplifies comparison of flow cytometry data for laboratories.
Making Precision Medicine a Reality
Researchers are one step closer to understanding the genetic and biological basis of diseases like cancer, diabetes, Alzheimer’s and rheumatoid arthritis – and identifying new drug targets and therapies.
New Database for Sharing MS Clinical Trial Data
A new database containing nearly 2500 patient records from the placebo arms of nine multiple sclerosis (MS) clinical trials is now available for research by qualified investigators.
‘Precision Prevention’ for Colorectal Cancer
New risk prediction model — not yet ready for clinical use — incorporates genetic, lifestyle and environmental risk factors.
Characterizing Cancerous Genomic Variations
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Uncovering Hidden Genomic Alterations that Drive Cancers
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
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