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Titlebook: Bioinformatics in Personalized Medicine; 10th Spanish Symposi Ana T. Freitas,Arcadi Navarro Conference proceedings 2012 Springer-Verlag Gmb

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jORCA and Magallanes Sailing Together towards Integration of Web Services,g with the discovery of data types, service composition (workflow generation) and refinement; to enactment, monitoring and visualization of results. The system has been exhaustively tested and documented and is freely available at ..
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0302-9743 dies; high-performanced databases; text-mining; tools for integration of Web services; ontologies; analysis and visualization of omics data.978-3-642-28061-0978-3-642-28062-7Series ISSN 0302-9743 Series E-ISSN 1611-3349
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https://doi.org/10.1007/978-1-4899-1869-7son. Our approach reproduces the expected behaviour and completes the proposal of Rost and Sander for homology based sequence comparisons. Results can be exploited by computational applications to reduce the computational cost and memory usage.
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Theories of Personality and Psychopathologysed on a holistic perspective of the genomic variation field, envisaging the integration of LSDBs, genes and variants, as well as a broad set of related resources in an innovative workspace. A prototype implementation for this approach is deployed online at ..
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https://doi.org/10.1007/978-0-230-20456-0 terms, EC numbers and KEEG pathways. It currently localises genes and transposons, which enable the sorting of contigs or scaffolds from a BAC clone, and reveals some putative assembly inconsistencies. Results are provided in GFF3 format and in tab-delimited text readable in viewers; a summary of findings is provided also as a PNG file.
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Statistical Significance for NGS Reads Similarities,son. Our approach reproduces the expected behaviour and completes the proposal of Rost and Sander for homology based sequence comparisons. Results can be exploited by computational applications to reduce the computational cost and memory usage.
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A Holistic Approach for Integrating Genomic Variation Information,sed on a holistic perspective of the genomic variation field, envisaging the integration of LSDBs, genes and variants, as well as a broad set of related resources in an innovative workspace. A prototype implementation for this approach is deployed online at ..
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