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March 2013
Scientific News
TAU Researchers Solve Disease Mystery Through Crowdfunding
Tel Aviv University researcher identifies novel genetic mutations through DNA sequencing of afflicted child and family.
A Gene That Shaped The Evolution Of Darwin's Finches
Researchers from Princeton University and Uppsala University in Sweden have identified a gene in the Galápagos finches studied by English naturalist Charles Darwin that influences beak shape and that played a role in the birds' evolution from a common ancestor more than 1 million years ago.
DNA ‘Cage’ Could Improve Nanopore Technology
Scientists at Brown University have designed a nanoscale cage that can trap a single DNA strand and allow before-and-after sequencing of the same DNA strand in research trials.
Epigenetic Signatures that Differentiate Triple-Negative Breast Cancers
Australian researchers have identified epigenetic ‘signatures’ that could help clinicians tell the difference between highly aggressive and more benign forms of triple-negative breast cancer.
New Techniques Reveal “Extreme” Gene Copy Range
New findings give scientists the first precise way to study places in the genome where the number of copies of a sequence varies widely from person to person.
New Software Analyzes Human Genomes Faster than Other Available Technologies
The new software will empower population scale genomic analysis.
Major Study Links Gene to Drug Resistance in Testicular Cancer
Researchers used a genetic technique called whole-exome sequencing to examine tumour samples.
Titin' Gene Mutations Will Help Identify Patients At Risk Of Heart Failure
A new study has identified genetic mutations that cause the heart condition dilated cardiomyopathy (DCM), paving the way for more accurate diagnosis.
Blood Test For Prostate Cancer
Vanderbilt team demonstrates that prostate cancer can accurately be detected by liquid biopsy.
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.
International Conference on Bioinformatics and Biomedicine (BIBM 2012)
04 Oct 2012 - 07 Oct 2013
Philadelphia, USA
International Conference on Bioinformatics and Biomedicine (BIBM 2012)
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12th Annual ePharma Summit
04 Mar 2013 - 06 Mar 2013
NY, USA
12th Annual ePharma Summit
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11 Mar 2013 - 13 Mar 2013
• Baltimore Hyatt • Baltimore, MD
5th Annual Government Programs Summit
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11 Mar 2013 - 15 Mar 2013
San Diego, CA, USA
Medicinal Chemistry 5-Day Program
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qPCR & NGS 2013 Event
18 Mar 2013 - 22 Mar 2013
Freising, Germany
qPCR & NGS 2013 Event
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19 Mar 2013 - 21 Mar 2013
Online
TM’s 2nd World Immunology Online Conference
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6th Oncology Biomarkers
20 Mar 2013 - 22 Mar 2013
San Francisco, CA, USA
6th Oncology Biomarkers
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Biomarkers Summit 2013
20 Mar 2013 - 22 Mar 2013
San Francisco, USA
Biomarkers Summit 2013
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NGS for Drugs, Patients and Clinical Trials
21 Mar 2013 - 22 Mar 2013
San Diego, CA, USA
NGS for Drugs, Patients and Clinical Trials
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