Nadav Ahituv
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Professor Nadav Ahituv is a faculty member at the University of California San Francisco, USA. His research encompasses genomic characterization, gene regulatory activity, and neurobiology, with recent publications focusing on topics such as human milk production, autism spectrum disorder, and the impact of transcription factor binding. He is also involved in the development of computational frameworks for optimizing sequence design strategies.
Recent Grants
Grant: Close
Massively parallel dissection of psychiatric regulatory networks
Open Date: 2016-05-01
Close Date: 2021-02-28
Grant: Close
Identification & functional characterization of SIM1 obesity-associated variants
Open Date: 2012-05-01
Close Date: 2016-03-31
Grant: Close
Massively parallel, in vivo functional testing of regulatory elements
Open Date: 2012-04-24
Close Date: 2015-06-30
Grant: Close
Characterization of neuronal gene regulatory elements associated with epilepsy
Open Date: 2012-04-01
Close Date: 2016-03-31
Grant: Close
Computational & Functional Annotation of the Zebrafish Genome Regulatory Toolbox
Open Date: 2009-09-29
Close Date: 2014-07-31
Articles (17)
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2025
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2025
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2025
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2025
The advent of perturbation-based massively parallel reporter assays (MPRAs) technique has facilitated the delineation of the roles of non-coding regulatory elements in orchestrating gene expression. However, computational efforts remain scant to evaluate and establish guidelines for sequence design strategies for perturbation MPRAs. In this study, we propose a framework for evaluating and comparing various perturbation strategies for MPRA experiments. Within this framework, we benchmark three different perturbation approaches from the perspectives of alteration in motif-based profiles, consistency of MPRA outputs, and robustness of models that predict the activities of putative regulatory motifs. While our analyses show very similar results across multiple benchmarking metrics, the predictive modeling for the approach involving random nucleotide shuffling shows significant robustness compared with the other two approaches. Thus, we recommend designing sequences by randomly shuffling the nucleotides of the perturbed site in perturbation-MPRA, followed by a coherence check to prevent the introduction of other variations of the target motifs. In summary, our evaluation framework and the benchmarking findings create a resource of computational pipelines and highlight the potential of perturbation-MPRA in predicting non-coding regulatory activities.
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2024
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2024
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2024
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2023
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2023
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2023
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2022
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2022
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2021
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2021
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2021
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2020
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2020
Collaborators (10)
Micaela Martinez
Assistant Professor
Emory University
Joon-Yong An
Assistant Professor
Korea University
Valerie Flaherman
Professor
University of California, San Francisco
Anat Kreimer
-
Fumitaka Inoue
Associate Professor
Kyoto University
Stephanie Gaw
University of California
Jason Klein
Assistant Professor
University of Colorado Cancer Center
Jay Shendure
Professor
University of Washington
Dmitri A Petrov
Stanford University
Stephan Sanders
Professor of Paediatric Neurogenetics
University of Oxford
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