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Spontaneous Mutations in Key Brain Gene are a Cause of Autism
In addition, there is a direct link between TBR1 and FOXP2, a well-known language-related protein, researchers report.
Leukemia Subtype Becomes More Common With Age
Genomic Analysis of 1,725 patients reveals the prevalence of Ph-like ALL increases with age.
Studies Reveal Diverse Molecular Mechanisms Underlying Evolution
Researchers have sequenced the genomes and transcriptomes of five species of African cichlid fishes and uncovered a variety of features that enabled the fishes to thrive in new habitats and ecological niches within the Great Lakes of East Africa.
New Gene Mutations for Wilms Tumor
UT Southwestern researchers identified the mutated genes by sequencing the DNA of 44 tumors.
New Sequence of Naked Mole Rat Genome Facilitates Cancer Resistance Research
Director of Science at The Genome Analysis Centre (TGAC) Federica Di Palma co-authors new genetic study on the naked mole rat’s resistance to cancer, identifying key genomic variations that may have contributed to the evolution of this extraordinary species.
Sequencing Identifies Gene Variant Responsible for Lupus
Research demonstrates it is feasible to identify the individual causes of lupus in patients by using DNA sequencing, allowing doctors to target specific treatments to individual patients.
“Deep sequencing” Picks up Hidden Causes of Brain Disorders
New approach complements whole-genome and whole-exome sequencing.
New Material Could Enhance Fast and Accurate DNA Sequencing
Nanopores in the material MoS2 sequence DNA more accurately, quickly and inexpensively.
ChIP Sequencing Kit for Next Generation Sequencing
The assay kit from Porvair Sciences extends the benefits of their proprietary Chromatrap® solid state ChIP technology.
Illumina's HiSeq X Ten Sequencing Technology for Population Studies
Next-generation sequencing technologies to be implemented at new High-Throughput Genomics Center for the MENA region.

Management of Genomic Big Data in a Country-wide Collaborative Initiative for Rare Disease Gene Finding.
Joaquin Dopazo, Centro De Investigacion Principe Felipe, speaking at Advances in NSG & Big Data 2014

Quantification of Bacterial DNA for Metagenomic Control Materials
Denise O'Sullivan, LGC Genomics, speaking at Advances in qPCR and dPCR

Lessons Learned from Implementing a National Infrastructure in Sweden for Storage and Analysis of Next-generation Sequencing Data
Ola Spjuth, Uppsala University, speaking at Advances in NGS & Big Data 2014

Can We Exploit the Power of NGS to Move Towards Personalized Medicine?
Jose Garcia Manteiga, San Raffaele Scientific Institute, Speaking at Advances in NGS & Big Data 2014

Automated Injection of Cancer Cells in 3D ECM Scaffolds and Zebrafish Embryos for (Personalized) Compound Screening
Jan De Sonneville, Life Science Methods B.V, speaking at High Content Analysis 2014

Use of Nextgen to Study Circulating Biomarkers
Mostafa Ronaghi, Illumina Inc, speaking at Exosomes and Circulating Biomarkers Summit 2013.

Unravelling Pathogen Virulence Strategies through the Application of Transcriptomics and Real-time Imaging
Professor Murray Grant, University of Exeter, speaking at AgriGenomics World Congress 2013.

Microvesicle (exosome) RNA as Biomarkers for Disease
Johan Skog, Exosome Diagnostics Inc, speaking at Exosomes and Circulating Biomarkers Summit 2013.

Next Generation Crop Genomics
Mario Caccamo, The Genome Analysis Centre, speaking at AgriGenomics World Congress 2013.

Automated Sequencing Analysis Tool for Infectious Disease Diagnostics
Robert Yamamoto, Zova Systems, speaking at Point-of-Care Diagnostics World Congress 2013.

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