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网友点评-Enografts. Journal of Experimental Clinical <a href="https://www.ncbi.nlm.nih.gov/pubmed/28242652" title=View Abstract(s)">PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/28242652-线缆测高仪,超声波测高仪, 手持式测高仪-上海交通大学科技园上海野豹企业发展公司
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Enografts. Journal of Experimental Clinical <a href="https://www.ncbi.nlm.nih.gov/pubmed/28242652" title=View Abstract(s)">PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/28242652
22 September 2008 Published: 27 August 2009 BMC Bioinformatics 2009, 10(Suppl 8):S6 doi:10.1186/1471-2105-10-S8-S <p>Proceedings on the European <a href="http://www.chemscene.com/13292-46-1.html">buy CS-2261</a> Conference on Computational Biology (ECCB) 2008 Workshop: Annotations, interpretation and management of mutations (AIMM)</p> Christopher JO Baker and Dietrich Rebholz-Schuhmann Research http://www.biomedcentral.com/content/pdf/1471-2105-10-S8-info.pdf This post is obtainable from: http://www.biomedcentral.com/1471-2105/10/S8/S6 ?2009 Bauer-Mehren et al; licensee BioMed Central Ltd. Final results: Very first, we identified the distinctive challenges posed by the integration from the phenotypic effect of sequence variants and mutations with biological networks. Second, we created a method for the mixture of information extracted from public resources, for example UniProt, NCBI dbSNP, Reactome and BioModels. We generated attribute files containing phenotypic and genotypic annotations for the nodes of biological networks, which can be imported into network visualization tools including Cytoscape. These sources permit the mapping and visualization of mutations and natural variations of human proteins and their phenotypic impact on.Enografts. Journal of Experimental Clinical Cancer Research 2012 31:61.Submit your next manuscript to BioMed Central and take full benefit of:?Practical on line submission ?Thorough peer assessment ?No space constraints or colour figure charges ?Quick publication on acceptance ?Inclusion in PubMed, CAS, Scopus and Google Scholar ?Investigation which is freely available for redistributionSubmit your manuscript at www.biomedcentral.com/submit
BMC BioinformaticsResearchBioMed CentralOpen AccessFrom SNPs to pathways: integration of functional impact of sequence variations on models of cell signalling pathwaysAnna Bauer-Mehren, Laura I Furlong*, Michael Rautschka and Ferran SanzAddress: Study Unit on Biomedical Informatics (GRIB), IMIM-Hospital del Mar, Universitat Pompeu Fabra. Barcelona Biomedical Analysis Park (PRBB) C/Dr. Aiguader, 88, 08003. Barcelona, Spain E-mail: Anna Bauer-Mehren - anna.bauer-mehren@upf.edu; Laura I Furlong* - lfurlong@imim.es; Michael Rautschka - mrautschka@imim.es; Ferran Sanz - fsanz@imim.es * Corresponding authorfrom ECCB 2008 Workshop: Annotations, interpretation and management of mutations (AIMM) Cagliari, Italy. 22 September 2008 Published: 27 August 2009 BMC Bioinformatics 2009, 10(Suppl eight):S6 doi:ten.1186/1471-2105-10-S8-S <p>Proceedings in the European Conference on Computational Biology (ECCB) 2008 Workshop: Annotations, interpretation and management of mutations (AIMM)</p> Christopher JO Baker and Dietrich Rebholz-Schuhmann Research http://www.biomedcentral.com/content/pdf/1471-2105-10-S8-info.pdf This short article is out there from: http://www.biomedcentral.com/1471-2105/10/S8/S6 ?2009 Bauer-Mehren et al; licensee BioMed Central Ltd. This really is an open access article distributed beneath the terms of the Inventive Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, supplied the original work is correctly cited.AbstractBackground: Single nucleotide polymorphisms (SNPs) would be the most frequent type of sequence variation among individuals, and represent a promising tool for obtaining genetic determinants of complicated illnesses and understanding the variations in drug response. In this regard, it is actually of specific interest to study the effect of non-synonymous SNPs within the context of biological networks such as cell signalling pathways. UniProt offers curated details about the functional and phenotypic effects of sequence variation, such as SNPs, too as on mutations of protein sequences.
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