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Biology subjects

Bowker, A.

Publications and source records attributed to Bowker, A..

3 recordsLinked to original sources

Automated detection, morphometric measurement, and size-class determination of harbor seals (Phoca vitulina) from UAV orthomosaics: a cascaded deep-learning pipeline with stratified validation across platforms, sensors, altitudes, and substrates

Reliable demographic data are critical for seal population assessment and management, yet remain challenging to obtain from drone surveys without automated tools. Using data from harbor seal (Phoca vitulina) haulout surveys conducted in British Columbia, Canada, in 2023-2024, we developed and tested an automated pipeline that integrates detection, morphometric extraction, and size-class classification of seals into a single system. The pipeline combines cascaded DeepLabV3+ segmentation (water removal, colony-level seal detection, and individual body-contour refinement), principal component analysis (PCA)-based extraction of body length and maximum width, and three-class size-class determination based on body length (pups, juveniles, subadults/adults). We evaluated the pipeline on 2,483 manually annotated seals across four drone platforms (DJI Mavic 3 Thermal, Mavic 2 Pro, Mini 3 Pro and Mini 2), five substrate types, and two sensor modalities (RGB, thermal infrared). Aggregate detection F1 was 0.914. Orthomosaic geometric accuracy, quantified as the RMSE of calibration-rod length on the orthomosaic, ranged from 1.0 cm to 18.0 cm depending on the platform-altitude-substrate combination, a spread that aggregate metrics would mask. Relative to manual annotation on the same orthomosaics, automated RGB body lengths showed near-zero bias (-0.6 cm; RMSE = 12.5 cm), whereas automated thermal lengths were systematically shorter (bias -19.9 cm, RMSE = 24.1 cm), establishing the unsuitability of thermal imagery for automated quantitative pinniped morphometry. For RGB imagery, threshold classification by body length reached an overall accuracy (OA) of 78.7%; for individuals outside the uncertainty zones (defined as {+/-}2 x the geometric RMSE on calibration rods around each class boundary), OA reached 90.9%. Within the RGB subset, OA was 78.9% at 20 m altitude, declining to 75.0% at 40 m where geometric error dominated. The pipeline enables automated demographic monitoring of pinniped haulouts with quantitatively characterized uncertainty across survey conditions.

ecology↗

Leukemia core transcriptional circuitry is a sparsely interconnected hierarchy stabilized by incoherent feed-forward loops

Lineage-defining transcription factors form densely interconnected circuits in chromatin occupancy assays, but the functional significance of these networks remains underexplored. We reconstructed the functional topology of a leukemia cell transcription network from the direct gene-regulatory programs of eight core transcriptional regulators established in pre-steady state assays coupling targeted protein degradation with nascent transcriptomics. The core regulators displayed narrow, largely non-overlapping direct transcriptional programs, forming a sparsely interconnected functional hierarchy stabilized by incoherent feed-forward loops. BET bromodomain and CDK7 inhibitors disrupted the core regulators direct programs, acting as mixed agonists/antagonists. The network is predictive of dynamic gene expression behaviors in time-resolved assays and clinically relevant pathway activity in patient populations.

systems biology↗

A distinct core regulatory module enforces oncogene expression in KMT2A-rearranged leukemia

A small set of lineage-restricted transcription factors (TFs), termed core regulatory circuitry (CRC), control cell identity and malignant transformation. Here, we integrated gene dependency, chromatin architecture and TF perturbation datasets to characterize 31 core TFs in acute myeloid leukemia (AML). Contrary to a widely accepted model, we detected a modular CRC structure with hierarchically organized, partially redundant and only sparsely interconnected modules of core TFs controlling distinct genetic programs. Rapid TF degradation followed by measurement of genome-wide transcription rates revealed that core TFs directly regulate dramatically fewer genes than previously assumed. Leukemias carrying KMT2A (MLL) rearrangements depend on the IRF8/MEF2 axis to directly enforce expression of the key oncogenes MYC, HOXA9 and BCL2. Our datasets provide an evolving model of CRC organization in human cells, and a resource for further inquiries into and therapeutic targeting of aberrant transcriptional circuits in cancer.

genomics↗