Kate E Binley1, Wai S Ng1, James R Tribble1, Bing Song2, James E Morgan3. 1. School of Optometry and Vision Sciences, Cardiff University, Maindy Road, Cardiff CF24 4LU, Wales, United Kingdom. 2. School of Dentistry, Cardiff University, Heath Park, Cardiff CF14 4XY, Wales, United Kingdom. 3. School of Optometry and Vision Sciences, Cardiff University, Maindy Road, Cardiff CF24 4LU, Wales, United Kingdom. Electronic address: MorganJE3@cf.ac.uk.
Abstract
BACKGROUND: Sholl analysis remains one of the most commonly used methods to quantify neuronal dendritic complexity and is therefore a key analysis tool in neurobiology. While initially proposed when the quantification of neuronal structure was undertaken manually, the advent of software packages allowing automated analysis has resulted in the introduction of several semi and fully automated methods to quantify dendritic complexity. Unfortunately results from these methods have not in all cases been consistent. We therefore compared the results of five commonly used methods (Simple Neurite Tracer, manual, Fast Sholl, Bitmap, and Ghosh lab) using manual analysis as a ground truth. NEW METHOD: Comparison of four semi-automated methods to the manual method using diolistically labelled mouse retinal ganglion cells. RESULTS: We report consistency across a range of published techniques. While the majority perform well (Simple Neurite Tracer and Fast Sholl profiles have areas under the curve within 4.5% of the profile derived using the manual method), we highlight two areas in two of the methods (Bitmap and Ghosh lab methods) where errors may occur, namely undercounting (>20% relative to the manual profile) and a second peak. COMPARISON WITH EXISTING METHODS: Our results support published validation of the Fast Sholl method. CONCLUSIONS: Our study highlights the importance of manual calibration of automated analysis software.
BACKGROUND: Sholl analysis remains one of the most commonly used methods to quantify neuronal dendritic complexity and is therefore a key analysis tool in neurobiology. While initially proposed when the quantification of neuronal structure was undertaken manually, the advent of software packages allowing automated analysis has resulted in the introduction of several semi and fully automated methods to quantify dendritic complexity. Unfortunately results from these methods have not in all cases been consistent. We therefore compared the results of five commonly used methods (Simple Neurite Tracer, manual, Fast Sholl, Bitmap, and Ghosh lab) using manual analysis as a ground truth. NEW METHOD: Comparison of four semi-automated methods to the manual method using diolistically labelled mouse retinal ganglion cells. RESULTS: We report consistency across a range of published techniques. While the majority perform well (Simple Neurite Tracer and Fast Sholl profiles have areas under the curve within 4.5% of the profile derived using the manual method), we highlight two areas in two of the methods (Bitmap and Ghosh lab methods) where errors may occur, namely undercounting (>20% relative to the manual profile) and a second peak. COMPARISON WITH EXISTING METHODS: Our results support published validation of the Fast Sholl method. CONCLUSIONS: Our study highlights the importance of manual calibration of automated analysis software.
Authors: Lu Deng; Sandra P Mojica-Perez; Ruth D Azaria; Mark Schultz; Jack M Parent; Wei Niu Journal: Mol Cell Neurosci Date: 2022-03-31 Impact factor: 4.626