Sponsorship & Exhibition
By attending this important event your company will:
Who will attend?
AstraZeneca is a research based pharmaceutical company.
In the area of oncology AstraZeneca is working to redefine the cancer treatment paradigm by delivering life-changing medicines to help address unmet clinical needs in a host of cancers and one day help eliminate the disease as a cause of death.https://www.astrazeneca.com/
PacBio® Single Molecule, Real-Time (SMRT®) Sequencing provides full access to human genomic variation through unmatched read length, uniform coverage and exceptional accuracy. With average reads lengths greater than 10 kb, PacBio DNA sequencing data reveals previously hidden structural variants and produces direct variant phasing information across haplotype blocks, in both whole genome and targeted applications. With SMRT Sequencing Systems, scientists gain new insight into the genetic basis of disease heritability and a more comprehensive view of human genetic variation.http://www.pacb.com/
Agena Bioscience is a San Diego, CA based life sciences and clinical diagnostics company that recently acquired the Bioscience business of Sequenom, Inc. and is now offering the MassARRAY® System. The system is a highly sensitive, quantitative method for nucleic acid detection via mass spectrometry for high-throughput genotyping and mutation profiling for cancer and other disease research, companion diagnostics, pharmacogenomics, molecular blood group typing, epigenetics, clinical genetics, agrigenomics, and molecular sample identification for bio-banking.http://agenabioscience.com/
Interactive Biosoftware is the creator of the Alamut® Software Suite offering a comprehensive solution to the complex tasks of genomic variants annotation, filtration, interpretation and reporting.
Sophia Genetics is the Global Leader in Data Driven Medicine. Our team of talented experts in Clinical Genomics, Machine Learning and Bioinformatics built Sophia DDM®, the most advanced analytical platform for clinical diagnostics. Over 175 leading hospitals use Sophia DDM® to diagnose thousands of patients each week in the fastest, most accurate possible way.http://www.sophiagenetics.com/home.html
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10x Genomics meets the critical need for long range, structural and cellular information, with an innovative system that transforms short-read sequencing technologies. Our Chromium™ System supports comprehensive genomics and high-throughput single cell transcriptomics. It enables researchers to discover previously inaccessible genomic information at unprecedented scale, including phased structural variants, phased single nucleotide variants, and dynamic gene expression of individual cells—while leveraging their existing sequencing systems and workflows.https://www.10xgenomics.com/
The Irys platform from BioNano Genomics provides unprecedented insights into whole-genome biology. Genome maps are generated from massively parallel single-molecule visualization of extremely long DNA. These maps provide dense genome-wide anchor points for ordering and orienting sequencing contigs or scaffolds to greatly increase completion and accuracy of de novo assemblies. Structural variants and repeats are measured directly within long “reads” for comprehensive analysis of what has been referred to as the inaccessible genome. For more see www.bionanogenomics.comhttp://www.bionanogenomics.com/
Phenosystems develops user-friendly software since 2002. Our software suite for molecular diagnostics comprises: GensearchNGS dedicated to mutation detection and interpretation on data from gene panels, Whole Exomes and Whole Genome; Gensearch for capillary DNA sequencing, GensearchGT Genotyping, GensearchHIV. Major features are high specificity and sensitivity, advanced tools to support variant interpretation (frameshifts, splice prediction, connection to LSDBs and to CaféVariome.org). All have been developed together with leading diagnostics laboratories in Europe, packing powerful tools in an extremely user friendly interface.
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Saphetor, the genome interpreter.
Saphetor provides end-to-end solution analysis for next generation DNA sequencing for research and clinical use. We seamlessly combine the world’s leading molecular databases, coupled with advanced software. To empower the research/medical professional to accurately identify the cause of cancer or genetic disease, and connect the patient to treatment options and clinical trials, we provide timely reports based on the most up-to-date information from academic and clinical research tailored to the patient's DNA data.
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Reference Laboratory Genetics is the Genetics and Molecular Diagnosis Division of ReferenceLaboratory.
It is nowadays the biggest laboratory of Genetics in Europe and guarantees the accomplishment of any genetic study required in his facilities with own resources.
The patient is our priority. We consider each case individually and suggest to carry on the most appropriate genetic studies.
All the genetic reports we issue are customized and are adapted to EMQN’s recommendations.
Our Head of Genetic Counselors is Dr. Esther Geán.http://reference-laboratory.es/
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