Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1093/bioinformatics/btw247 http://scihub22266oqcxt.onion/10.1093/bioinformatics/btw247 C4908331!4908331 !27307649     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27307649 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Bioinformatics 2016 ; 32 (12 ): i90-i100 Nephropedia Template TP {{tp|p=27307649 |t=2016. Jumping across biomedical contexts using compressive data fusion |pdf=|usr=}}{{27307649 }} gab.com Text Jumping across biomedical contexts using compressive data fusion JO: Bioinformatics http://www.kidney.de/pget.php?&tw=1&pmid=27307649 #FOAvip MOTIVATION: The rapid growth of diverse biological data allows us to consider interactions between a variety of objects, such as genes, chemicals, molecular signatures, diseases, pathways and environmental exposures. Often, any pair of objects-such as a gene and a disease-can be related in different ways, for example, directly via gene-disease associations or indirectly via functional annotations, chemicals and pathways. Different ways of relating these objects carry different semantic meanings However, traditional methods disregard these semantics and thus cannot fully exploit their value in data modeling. RESULTS: We present Medusa, an approach to detect size-k modules of objects that, taken together, appear most significant to another set of objects. Medusa operates on large-scale collections of heterogeneous datasets and explicitly distinguishes between diverse data semantics. It advances research along two dimensions: it builds on collective matrix factorization to derive different semantics, and it formulates the growing of the modules as a submodular optimization program. Medusa is flexible in choosing or combining semantic meanings and provides theoretical guarantees about detection quality. In a systematic study on 310 complex diseases, we show the effectiveness of Medusa in associating genes with diseases and detecting disease modules. We demonstrate that in predicting gene-disease associations Medusa compares favorably to methods that ignore diverse semantic meanings. We find that the utility of different semantics depends on disease categories and that, overall, Medusa recovers disease modules more accurately when combining different semantics. AVAILABILITY AND IMPLEMENTATION: Source code is at http://github.com/marinkaz/medusa CONTACT: marinka@cs.stanford.edu, blaz.zupan@fri.uni-lj.si. Twit Text FOAVip Jumping across biomedical contexts using compressive data fusion ????Bioinformatics http://www.kidney.de/pget.php?&tw=1&pmid=27307649 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27307649 #FOAvip English Wikipedia <ref>{{Cite pmid|27307649 }}</ref> Jumping across biomedical contexts using compressive data fusion #MMPMID27307649 Zitnik M ; Zupan B Bioinformatics 2016[Jun]; 32 (12 ): i90-i100 PMID27307649 show ga MOTIVATION: The rapid growth of diverse biological data allows us to consider interactions between a variety of objects, such as genes, chemicals, molecular signatures, diseases, pathways and environmental exposures. Often, any pair of objects-such as a gene and a disease-can be related in different ways, for example, directly via gene-disease associations or indirectly via functional annotations, chemicals and pathways. Different ways of relating these objects carry different semantic meanings However, traditional methods disregard these semantics and thus cannot fully exploit their value in data modeling. RESULTS: We present Medusa, an approach to detect size-k modules of objects that, taken together, appear most significant to another set of objects. Medusa operates on large-scale collections of heterogeneous datasets and explicitly distinguishes between diverse data semantics. It advances research along two dimensions: it builds on collective matrix factorization to derive different semantics, and it formulates the growing of the modules as a submodular optimization program. Medusa is flexible in choosing or combining semantic meanings and provides theoretical guarantees about detection quality. In a systematic study on 310 complex diseases, we show the effectiveness of Medusa in associating genes with diseases and detecting disease modules. We demonstrate that in predicting gene-disease associations Medusa compares favorably to methods that ignore diverse semantic meanings. We find that the utility of different semantics depends on disease categories and that, overall, Medusa recovers disease modules more accurately when combining different semantics. AVAILABILITY AND IMPLEMENTATION: Source code is at http://github.com/marinkaz/medusa CONTACT: marinka@cs.stanford.edu, blaz.zupan@fri.uni-lj.si. |*Data Compression [MESH] |*Semantics [MESH] |Algorithms [MESH] |Computational Biology/*methods [MESH] |Disease/*genetics [MESH] |Gene Ontology [MESH]Jumping across biomedical contexts using compressive data fusion (epmc).pdf DeepDyve Pubget Overpricing