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  1. Article ; Online: Contextual Hub Analysis Tool (CHAT)

    Tanja Muetze / Ivan H. Goenawan / Heather L. Wiencko / Manuel Bernal-Llinares / Kenneth Bryan / David J. Lynn

    F1000Research, Vol

    A Cytoscape app for identifying contextually relevant hubs in biological networks [version 2; referees: 2 approved]

    2016  Volume 5

    Abstract: Highly connected nodes (hubs) in biological networks are topologically important to the structure of the network and have also been shown to be preferentially associated with a range of phenotypes of interest. The relative importance of a hub node, ... ...

    Abstract Highly connected nodes (hubs) in biological networks are topologically important to the structure of the network and have also been shown to be preferentially associated with a range of phenotypes of interest. The relative importance of a hub node, however, can change depending on the biological context. Here, we report a Cytoscape app, the Contextual Hub Analysis Tool (CHAT), which enables users to easily construct and visualize a network of interactions from a gene or protein list of interest, integrate contextual information, such as gene expression or mass spectrometry data, and identify hub nodes that are more highly connected to contextual nodes (e.g. genes or proteins that are differentially expressed) than expected by chance. In a case study, we use CHAT to construct a network of genes that are differentially expressed in Dengue fever, a viral infection. CHAT was used to identify and compare contextual and degree-based hubs in this network. The top 20 degree-based hubs were enriched in pathways related to the cell cycle and cancer, which is likely due to the fact that proteins involved in these processes tend to be highly connected in general. In comparison, the top 20 contextual hubs were enriched in pathways commonly observed in a viral infection including pathways related to the immune response to viral infection. This analysis shows that such contextual hubs are considerably more biologically relevant than degree-based hubs and that analyses which rely on the identification of hubs solely based on their connectivity may be biased towards nodes that are highly connected in general rather than in the specific context of interest. Availability: CHAT is available for Cytoscape 3.0+ and can be installed via the Cytoscape App Store (http://apps.cytoscape.org/apps/chat).
    Keywords Bioinformatics ; Tropical & Travel-Associated Diseases ; Medicine ; R ; Science ; Q
    Subject code 572
    Language English
    Publishing date 2016-08-01T00:00:00Z
    Publisher F1000 Research Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRASG13D

    Susan A. Kennedy / Mohamed-Ali Jarboui / Sriganesh Srihari / Cinzia Raso / Kenneth Bryan / Layal Dernayka / Theodosia Charitou / Manuel Bernal-Llinares / Carlos Herrera-Montavez / Aleksandar Krstic / David Matallanas / Max Kotlyar / Igor Jurisica / Jasna Curak / Victoria Wong / Igor Stagljar / Thierry LeBihan / Lisa Imrie / Priyanka Pillai /
    Miriam A. Lynn / Erik Fasterius / Cristina Al-Khalili Szigyarto / James Breen / Christina Kiel / Luis Serrano / Nora Rauch / Oleksii Rukhlenko / Boris N. Kholodenko / Luis F. Iglesias-Martinez / Colm J. Ryan / Ruth Pilkington / Patrizia Cammareri / Owen Sansom / Steven Shave / Manfred Auer / Nicola Horn / Franziska Klose / Marius Ueffing / Karsten Boldt / David J. Lynn / Walter Kolch

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 14

    Abstract: Kras is often mutated in colorectal cancer but how this oncogenic mutation alters signalling pathways globally is undetermined. Here, the authors analyse how this mutation affects protein interaction networks and signal flow showing an extensive re‐ ... ...

    Abstract Kras is often mutated in colorectal cancer but how this oncogenic mutation alters signalling pathways globally is undetermined. Here, the authors analyse how this mutation affects protein interaction networks and signal flow showing an extensive re‐wiring of signalling in response to KRas mutation
    Keywords Science ; Q
    Language English
    Publishing date 2020-01-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRASG13D

    Susan A. Kennedy / Mohamed-Ali Jarboui / Sriganesh Srihari / Cinzia Raso / Kenneth Bryan / Layal Dernayka / Theodosia Charitou / Manuel Bernal-Llinares / Carlos Herrera-Montavez / Aleksandar Krstic / David Matallanas / Max Kotlyar / Igor Jurisica / Jasna Curak / Victoria Wong / Igor Stagljar / Thierry LeBihan / Lisa Imrie / Priyanka Pillai /
    Miriam A. Lynn / Erik Fasterius / Cristina Al-Khalili Szigyarto / James Breen / Christina Kiel / Luis Serrano / Nora Rauch / Oleksii Rukhlenko / Boris N. Kholodenko / Luis F. Iglesias-Martinez / Colm J. Ryan / Ruth Pilkington / Patrizia Cammareri / Owen Sansom / Steven Shave / Manfred Auer / Nicola Horn / Franziska Klose / Marius Ueffing / Karsten Boldt / David J. Lynn / Walter Kolch

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 14

    Abstract: Kras is often mutated in colorectal cancer but how this oncogenic mutation alters signalling pathways globally is undetermined. Here, the authors analyse how this mutation affects protein interaction networks and signal flow showing an extensive re‐ ... ...

    Abstract Kras is often mutated in colorectal cancer but how this oncogenic mutation alters signalling pathways globally is undetermined. Here, the authors analyse how this mutation affects protein interaction networks and signal flow showing an extensive re‐wiring of signalling in response to KRas mutation
    Keywords Science ; Q
    Language English
    Publishing date 2020-01-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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