MonStim Analyzer — Project Write-up
Published:
A production PyQt6 desktop application for processing, visualizing, and analyzing 100+ GB multi-channel electrophysiological datasets — reducing lab analysis time by ~80%.
Published:
A production PyQt6 desktop application for processing, visualizing, and analyzing 100+ GB multi-channel electrophysiological datasets — reducing lab analysis time by ~80%.
Published:
Adapting and publishing a MATLAB spatial interpolation toolkit as the open-source, reproducible analysis pipeline for a peer-reviewed eLife study on spinal interneuron distributions.
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A companion PyQt6 application for automated, reproducible generation of publication-quality EMG trace figures — turning a half-day manual task into a 10-minute batch job.
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A normalized SQLite database built on PubMed open data, with a Python ETL pipeline and five analytical SQL queries mapping publication trends in spinal neuroscience.
Published in Emory Theses and Dissertations (ETD), 2020
Undergraduate Honors Thesis.
Recommended citation: Worthy, A. (2020) Spiteful Weapons and the Environmental Dependence of Phage. Honors Thesis. Emory University. Available at: https://etd.library.emory.edu/concern/etds/bv73c164v?locale=en.
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Published in FEMS Microbiology Ecology, 2020
This study demonstrates that overproduction of exopolysaccharides, “mucoidy”, allows bacterial populations to be resistant to lytic bacteriophage infection. We found that spontaneous reversion from the mucoid state to the susceptible non-mucoid state allows these phage-resistant bacterial populations to maintain lytic viruses without greatly affecting the bacterial population density.
Recommended citation: Waqas Chaudhry, Esther Lee, Andrew Worthy, Zoe Weiss, Marcin Grabowicz, Nicole Vega, Bruce Levin, Mucoidy, a general mechanism for maintaining lytic phage in populations of bacteria, FEMS Microbiology Ecology, Volume 96, Issue 10, October 2020, fiaa162, https://doi.org/10.1093/femsec/fiaa162
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Published in eLife, 2024
This study characterizes the various subtypes (“clades”) of spinal V1 interneurons, describing their relative neurogenesis times, their distributions throughout the lumbar spinal cord, and their connections to motoneurons. It also investigates the molecular identities of further subdivisions within the Foxp2-V1 clade, and demonstrates that some of these Foxp2-V1s have connectivity that resembles reciprocal Ia inhibitory interneurons (IaINs).
Recommended citation: Andrew E Worthy, Joanna T Anderson, Alicia R Lane, Laura J Gomez-Perez, Anthony A Wang, Ronald W Griffith, Andre F Rivard, Jay B Bikoff, Francisco J Alvarez (2024) Spinal V1 inhibitory interneuron clades differ in birthdate, projections to motoneurons, and heterogeneity eLife 13:RP95172. https://doi.org/10.7554/eLife.95172.3
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Published in bioRxiv (preprint), 2026
This study uses optogenetics with a fast channelrhodopsin variant (CatCh) to reveal how temporal patterns and synchrony of activity within Aβ low threshold mechanoreceptor subtypes control signal propagation to primary somatosensory cortex. We found that sustained cortical responses require synchronous activation of multiple Aβ SAI-LTMRs, while Aβ RAI-LTMRs drive robust cortical responses even with asynchronous activation.
Recommended citation: Wanyi Liu, Andrew E. Worthy, Alan J. Emanuel (2026). Synchrony within Aβ mechanoreceptor subtypes governs signal propagation to primary somatosensory cortex. bioRxiv. https://doi.org/10.64898/2026.01.16.700009
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Published:
Presented research findings on the heterogeneity of spinal V1 interneurons expressing the transcription factor Foxp2. This work contributed to our understanding of how V1 interneuron clades differ in their molecular identities and functional roles in the spinal cord.
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Presented poster describing the molecular heterogeneity of the Foxp2-expressing V1 interneuron clade in the spinal cord, revealing multiple discrete subpopulations with distinct connectivity patterns. Work contributed to the eLife publication (Worthy et al. 2024).
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Presented poster reporting that selective Renshaw cell ablation increases monosynaptic H-reflex amplitude in the decerebrate mouse preparation, providing direct evidence for Renshaw cell-mediated recurrent inhibition of the H-reflex pathway.
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Presented ongoing research investigating how Renshaw cells modulate reciprocal inhibition pathways and influence motor output. This work combines in vivo electrophysiology with computational modeling to elucidate the functional roles of Renshaw cells in spinal motor circuits.
Undergraduate course, Emory University, Biology Department, 2024
Role: Graduate Teaching Assistant