TY - JOUR
T1 - Interactive Big Data Resource to Elucidate Human Immune Pathways and Diseases
AU - Gorenshteyn, Dmitriy
AU - Zaslavsky, Elena
AU - Fribourg, Miguel
AU - Park, Christopher Y.
AU - Wong, Aaron K.
AU - Tadych, Alicja
AU - Hartmann, Boris M.
AU - Albrecht, Randy A.
AU - García-Sastre, Adolfo
AU - Kleinstein, Steven H.
AU - Troyanskaya, Olga G.
AU - Sealfon, Stuart C.
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/9/15
Y1 - 2015/9/15
N2 - Many functionally important interactions between genes and proteins involved in immunological diseases and processes are unknown. The exponential growth in public high-throughput data offers an opportunity to expand this knowledge. To unlock human-immunology-relevant insight contained in the global biomedical research effort, including all public high-throughput datasets, we performed immunological-pathway-focused Bayesian integration of a comprehensive, heterogeneous compendium comprising 38,088 genome-scale experiments. The distillation of this knowledge into immunological networks of functional relationships between molecular entities (ImmuNet), and tools to mine this resource, are accessible to the public at http://immunet.princeton.edu. The predictive capacity of ImmuNet, established by rigorous statistical validation, is easily accessed by experimentalists to generate data-driven hypotheses. We demonstrate the power of this approach through the identification of unique host-virus interaction responses, and we show how ImmuNet complements genetic studies by predicting disease-associated genes. ImmuNet should be widely beneficial for investigating the mechanisms of the human immune system and immunological diseases. The large amount of publically available high-throughput data contains, in aggregate, a vast amount of immunologically relevant insight. Sealfon and colleagues report ImmuNet, a web-accessible public resource based on 38,088 experiments that allows researchers to predict gene-gene relationships relevant to the human immune system and immunological diseases.
AB - Many functionally important interactions between genes and proteins involved in immunological diseases and processes are unknown. The exponential growth in public high-throughput data offers an opportunity to expand this knowledge. To unlock human-immunology-relevant insight contained in the global biomedical research effort, including all public high-throughput datasets, we performed immunological-pathway-focused Bayesian integration of a comprehensive, heterogeneous compendium comprising 38,088 genome-scale experiments. The distillation of this knowledge into immunological networks of functional relationships between molecular entities (ImmuNet), and tools to mine this resource, are accessible to the public at http://immunet.princeton.edu. The predictive capacity of ImmuNet, established by rigorous statistical validation, is easily accessed by experimentalists to generate data-driven hypotheses. We demonstrate the power of this approach through the identification of unique host-virus interaction responses, and we show how ImmuNet complements genetic studies by predicting disease-associated genes. ImmuNet should be widely beneficial for investigating the mechanisms of the human immune system and immunological diseases. The large amount of publically available high-throughput data contains, in aggregate, a vast amount of immunologically relevant insight. Sealfon and colleagues report ImmuNet, a web-accessible public resource based on 38,088 experiments that allows researchers to predict gene-gene relationships relevant to the human immune system and immunological diseases.
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U2 - 10.1016/j.immuni.2015.08.014
DO - 10.1016/j.immuni.2015.08.014
M3 - Article
C2 - 26362267
AN - SCOPUS:84941733052
SN - 1074-7613
VL - 43
SP - 605
EP - 614
JO - Immunity
JF - Immunity
IS - 3
M1 - 3157
ER -