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Genedata releases a breakthrough for genomic comparison -Genedata Selector4.0 provides reference-independent genome sequence comparisons while reducing data processing and analysis time to optimize efficiency and save costs
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Genedata releases a breakthrough for genomic comparison -Genedata Selector4.0 provides reference-independent genome sequence comparisons while reducing data processing and analysis time to optimize efficiency and save costs
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Publish time:
21
st
July, 2015
Source:
Basel,Switzerland
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Genedata releases a breakthrough for genomic comparison -Genedata Selector4.0 provides reference-independent genome sequence comparisons while reducing data processing and analysis time to optimize efficiency and save costsGenedata releases a breakthrough for genomic comparison -Genedata Selector4.0 provides reference-independent genome sequence comparisons while reducing data processing and analysis time to optimize efficiency and save costs" title="Share this link on Facebook">Basel,SwitzerlandJuly 21, 2015Genedata,a leading provider of advanced software solutions for agribusiness,
industrial biotechnology
, pharmaceuticals and related life science research, today announced the release of Genedata Selector 4.0. This latest version of the industry's leading genome knowledge management solution provides groundbreaking new capabilities for reference-independent genome sequence comparisons while reducing data processing and analysis time. Genedata Selector 4.0's powerful new comparative genomics functionalities make it possible for the first time to compare and interpret genomic variants across assemblies and sequencing approaches. At the same time, the new automated processing pipeline optimizes user efficiency and lowers costs throughout the workflow, from integrating new knowledge, maintaining existing knowledge and interpreting data to generating reports.First-In-Class Reference-Independent Genomic Comparison and Analyses Across Lineages: Genedata Selector 4.0 Addresses Current ChallengesHigh-quality reference genomes serve important roles in identifying and understanding genomic variants across strains and lines. As new reference assemblies become available over time, organizations are faced with a significant challenge in order to retain existing knowledge and integrate it with the new references. Information from past analyses and the related intellectual property is often lost or dispersed over time, and no longer available for use in the discovery process. For researchers, the comparison of variants across reference systems is a difficult and time-consuming task, while for bioinformaticians, the re-alignment of historic data to new reference genomes is a challenge. Other data management systems that store variants relative to reference assemblies do not enable the performance of analyses that span different reference systems, or between genomes that are assembled without a reference genome (for example, de novo sequencing methods). Keeping all of the constantly accumulating variant knowledge current and accurate involves vast amounts of data, placing high demands on hardware and IT resources. As sequencing costs decrease and de novo sequencing approaches become more prevalent, there is a pressing need for knowledge management solutions with fewer limitations which reduce pressure on resources.Genedata Selector 4.0 has been specially designed to meet these challenges. New genome assemblies and re-sequenced genomes can now be easily integrated with existing genomic knowledge through a new processing pipeline which automatically updates variant data from previous analyses. Users now have the ability to analyze genomic sequences and protein affects across any available reference assembly. This includes choosing a reference from within the user interface, or directly comparing variants independent of any reference genome.Highlights of the new version of Genedata Selector:Efficient, flexible management of variant dataAn automated and scalable processing pipeline for easy integration of new genomes and calculation of genomic sequence differencesInteractive exploration, comparison and fast interpretation of genomic variant informationQuerying and analysis of variant knowledge with no restrictions on the reference genome or sequencing approach usedThese new features are tightly integrated with the robust knowledge management and data analysis capabilities of the platform - capabilities currently valued by customers across a wide range of industries. Within a single, integrated framework, Genedata Selector manages and analyzes genome-related data for strain and cell line optimization."We are very proud to provide organizations with unique functionalities integrated in a single platform to generate new insights into their data while creating efficiencies and reducing costs," said Dr. Othmar Pfannes, CEO of Genedata. "With version 4.0, we enable researchers to fully leverage the most advanced
technologies
used in genome-based research and we are firmly committed to continually advancing this platform to meet their emerging needs."About GenedataGenedata transforms data into intelligence with a portfolio of advanced software solutions, which make research data accessible and understandable and research processes more efficient. These solutions are used worldwide by leading pharmaceutical, industrial, and agricultural biotechnology companies as well as academic research organizations. Genedata innovations enable scientific discovery that fights disease and improves health and quality of life worldwide. Founded in 1997, Genedata is headquartered in Switzerland, and has offices in Germany, Japan, and the US.More news from: Genedata AGWebsite: http://www.cnchemicals.com/: July 21, 2015The news item on this page is copyright by the organization where it originatedFair use notice
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