Nadav Ahituv

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Professor

University of California, San Francisco
Country flagUnited States

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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

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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

UNITED STATES
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Joon-Yong An

Assistant Professor

Korea University

SOUTH KOREA
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Valerie Flaherman

Professor

University of California, San Francisco

UNITED STATES
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Anat Kreimer

-

UNITED STATES
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Fumitaka Inoue

Associate Professor

Kyoto University

JAPAN
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Stephanie Gaw

University of California

UNITED STATES
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Jason Klein

Assistant Professor

University of Colorado Cancer Center

UNITED STATES
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Jay Shendure

Professor

University of Washington

UNITED STATES
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Dmitri A Petrov

Stanford University

UNITED STATES
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Stephan Sanders

Professor of Paediatric Neurogenetics

University of Oxford

UNITED KINGDOM
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