6 results match your criteria: "USA. [3] Simons Center for Data Analysis[Affiliation]"

A global genetic interaction network maps a wiring diagram of cellular function.

Science

September 2016

The Donnelly Centre, University of Toronto, 160 College Street, Toronto ON, Canada M5S 3E1. Department of Molecular Genetics, University of Toronto, 160 College Street, Toronto ON, Canada M5S 3E1. Chemical Genomics Research Group, RIKEN Center for Sustainable Resource Sciences (CSRS), Saitama, Japan.

Article Synopsis
  • The researchers created a global genetic interaction network for yeast, generating over 23 million double mutants to identify around 550,000 negative and 350,000 positive genetic interactions.
  • The network highlights essential genes as key connectors and allows for the assembly of a hierarchical model that represents various aspects of cell function, including protein complexes and biological processes.
  • Negative interactions link related genes and core biological processes, while positive interactions reflect broader regulatory connections, ultimately forming a functional wiring diagram of the cell.
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Identification of multi-loci hubs from 4C-seq demonstrates the functional importance of simultaneous interactions.

Nucleic Acids Res

October 2016

Interdepartmental Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06511, USA Department of Pathology and Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USA Program of Applied Mathematics, Yale university, New Haven, CT, USA

Use of low resolution single cell DNA FISH and population based high resolution chromosome conformation capture techniques have highlighted the importance of pairwise chromatin interactions in gene regulation. However, it is unlikely that associations involving regulatory elements act in isolation of other interacting partners that also influence their impact. Indeed, the influence of multi-loci interactions remains something of an enigma as beyond low-resolution DNA FISH we do not have the appropriate tools to analyze these.

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Helminth infection promotes colonization resistance via type 2 immunity.

Science

April 2016

Kimmel Center for Biology and Medicine at the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA. Departments of Microbiology and Medicine, New York University School of Medicine, New York, NY 10016, USA.

Increasing incidence of inflammatory bowel diseases, such as Crohn's disease, in developed nations is associated with changes to the microbial environment, such as decreased prevalence of helminth colonization and alterations to the gut microbiota. We find that helminth infection protects mice deficient in the Crohn's disease susceptibility gene Nod2 from intestinal abnormalities by inhibiting colonization by an inflammatory Bacteroides species. Resistance to Bacteroides colonization was dependent on type 2 immunity, which promoted the establishment of a protective microbiota enriched in Clostridiales.

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Robust classification of protein variation using structural modelling and large-scale data integration.

Nucleic Acids Res

April 2016

Department of Biology, New York University, New York, NY 10003, USA New York University Center for Genomics and Systems Biology, New York, NY 10003, USA Computer Science Department, New York University, New York, NY 10003, USA Simons Center for Data Analysis, Simons Foundation, New York, NY 10010, USA Simons Foundation, New York, NY 10010, USA

Existing methods for interpreting protein variation focus on annotating mutation pathogenicity rather than detailed interpretation of variant deleteriousness and frequently use only sequence-based or structure-based information. We present VIPUR, a computational framework that seamlessly integrates sequence analysis and structural modelling (using the Rosetta protein modelling suite) to identify and interpret deleterious protein variants. To train VIPUR, we collected 9477 protein variants with known effects on protein function from multiple organisms and curated structural models for each variant from crystal structures and homology models.

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IMP 2.0: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks.

Nucleic Acids Res

July 2015

Department of Computer Science, Princeton University, Princeton, NJ 08540, USA Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08540, USA Simons Center for Data Analysis, Simons Foundation, NY 10010, USA

IMP (Integrative Multi-species Prediction), originally released in 2012, is an interactive web server that enables molecular biologists to interpret experimental results and to generate hypotheses in the context of a large cross-organism compendium of functional predictions and networks. The system provides biologists with a framework to analyze their candidate gene sets in the context of functional networks, expanding or refining their sets using functional relationships predicted from integrated high-throughput data. IMP 2.

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FNTM: a server for predicting functional networks of tissues in mouse.

Nucleic Acids Res

July 2015

Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08540, USA Simons Center for Data Analysis, Simons Foundation, NY 10010, USA Department of Computer Science, Princeton University, Princeton, NJ 08540, USA

Functional Networks of Tissues in Mouse (FNTM) provides biomedical researchers with tissue-specific predictions of functional relationships between proteins in the most widely used model organism for human disease, the laboratory mouse. Users can explore FNTM-predicted functional relationships for their tissues and genes of interest or examine gene function and interaction predictions across multiple tissues, all through an interactive, multi-tissue network browser. FNTM makes predictions based on integration of a variety of functional genomic data, including over 13 000 gene expression experiments, and prior knowledge of gene function.

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