The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Revealing the structure of pharmacobehavioral space through motion sequencing
Open accessAbstract
Understanding how genes, drugs and neural circuits influence behavior requires the ability to effectively organize information about similarities and differences within complex behavioral datasets. Motion Sequencing (MoSeq) is an ethologically inspired behavioral analysis method that identifies modular components of three-dimensional mouse body language called ‘syllables’. Here, we show that MoSeq effectively parses behavioral differences and captures similarities elicited by a panel of neuroactive and psychoactive drugs administered to a cohort of nearly 700 mice. MoSeq identifies syllables that are characteristic of individual drugs, a finding we leverage to reveal specific on- and off-target effects of both established and candidate therapeutics in a mouse model of autism spectrum disorder. These results demonstrate that MoSeq can meaningfully organize large-scale behavioral data, illustrate the power of a fundamentally modular description of behavior and suggest that behavioral syllables represent a new class of druggable target. By analyzing hundreds of mice treated with a library of neuro- and psychoactive drugs, Wiltschko et al. show that Motion Sequencing can effectively discriminate and categorize drug effects and link molecular targets to behavioral syllables.
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Cites
DeepLabCut: markerless pose estimation of user-defined body parts with deep learning
Mathis, A., Mamidanna, P., Cury, K. M., Abe, T., Murthy, V. N., Mathis, M. W., & Bethge, M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0209-y · Cited by 5,187
Rowan, W., & Tinbergen, N. (1952) · Bird-Banding · doi:10.2307/4510368 · Cited by 2,696
How were new medicines discovered?
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Genetics of Mouse Behavior: Interactions with Laboratory Environment
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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., Sebat, J., Wigler, M., Martin, C. L., Ledbetter, D. H., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.09.005 · Cited by 818 · cited 1×
“To explore this possibility, we used MoSeq to phenotype mice harboring a mutation in the CNTNAP2 gene, which is associated with human ASD 20,29,30 .”
MethodMapping Sub-Second Structure in Mouse Behavior
Wiltschko, A. B., Johnson, M. J., Iurilli, G., Peterson, R. E., Katon, J. M., Pashkovski, S. L., Abraira, V. E., Adams, R. P., & Datta, S. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.11.031 · Cited by 760
Self-citationFast animal pose estimation using deep neural networks
Pereira, T. D., Aldarondo, D. E., Willmore, L., Kislin, M., Wang, S. S.-H., Murthy, M., & Shaevitz, J. W. (2019) · Nature Methods · doi:10.1038/s41592-018-0234-5 · Cited by 687
Mapping the stereotyped behaviour of freely moving fruit flies
Berman, G. J., Choi, D. M., Bialek, W., & Shaevitz, J. W. (2014) · Journal of The Royal Society Interface · doi:10.1098/rsif.2014.0672 · Cited by 565
Cited by
Keypoint-MoSeq: parsing behavior by linking point tracking to pose dynamics
Weinreb, C., Pearl, J. E., Lin, S., Osman, M. A. M., Zhang, L., Annapragada, S., Conlin, E., Hoffmann, R., Makowska, S., Gillis, W. F., et al. (2024) · Nature Methods · doi:10.1038/s41592-024-02318-2 · Cited by 228
Self-citationMeasuring behavior in the home cage: study design, applications, challenges, and perspectives
Grieco, F., Bernstein, B. J., Biemans, B., Bikovski, L., Burnett, C. J., Cushman, J. D., van Dam, E. A., Fry, S. A., Richmond-Hacham, B., Homberg, J. R., et al. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.735387 · Cited by 109
Open-source tools for behavioral video analysis: Setup, methods, and best practices
Luxem, K., Sun, J. J., Bradley, S. P., Krishnan, K., Yttri, E., Zimmermann, J., Pereira, T. D., & Laubach, M. (2023) · eLife · doi:10.7554/elife.79305 · Cited by 98
Neural circuits regulating prosocial behaviors
Walsh, J. J., Christoffel, D. J., & Malenka, R. C. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-022-01348-8 · Cited by 72
Behavioral decomposition reveals rich encoding structure employed across neocortex in rats
Mimica, B., Tombaz, T., Battistin, C., Fuglstad, J. G., Dunn, B. A., & Whitlock, J. R. (2023) · Nature Communications · doi:10.1038/s41467-023-39520-3 · Cited by 45
Metadata
- Authors
- Wiltschko, A. B., Tsukahara, T., Zeine, A., Anyoha, R., Gillis, W. F., Markowitz, J. E., Peterson, R. E., Katon, J., Johnson, M. J., & Datta, S. R.
- Venue
- Nature Neuroscience
- Published
- 2020-09-21
- Volume
- 23
- Issue
- 11
- Pages
- 1433-1443
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W3087056597
- Cited by
- 298
- References
- 37
- FWCI
- 12.96
- Type
- journal article
- Language
- en
- Open access
- green
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