Saturday, January 31, 2015
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16S rRNA Amplicon Sequencing Offers Enhanced Metagenomic Detection
Accelerating Bioinformatics Searching and Dot Plotting Using a Scalabl
IBM eX5 Improves Next Generation Sequencing for Sanger Institute
Next-Generation Data Storage
Next-generation sequencing of highly multiplexed samples: the NuGEN En
NuGEN Technologies, Inc.
Overview of NGS Applications in Bioprocess Development, Scale-up, and
Randomized Adapters for Reducing Bias in Small RNA-Seq Libraries
RNA-Seq Data Comparison with Gene Expression Microarrays
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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.
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.
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