Journal: Biophysical Reports
Article Title: ATLAS: Machine learning-enhanced filament analysis for the In Vitro Motility Assay
doi: 10.1016/j.bpr.2025.100221
Figure Lengend Snippet: Filament tracking challenges and number of analyzable tracks. ( A ) Small filaments, moving at fast velocities, become untrackable as filament detection overlap ( red shaded area on left ) falls below cutoff values for Deep SORT. ( B ) Example of identity switching. Two filaments identified as ID 1 and ID 2 moving slowly between frames, t to t + 3. Their identities are switched when YOLOv5 detects the two filaments as a single object (frame t + 2). Resolution of this causes the Deep SORT track of the lower filament ( ID 2 ) to transition from the lower filament in frame t to the upper filament in frame t + 3 . In extremely slow-motion conditions, this introduces a large, incorrect displacement into this filament’s track, resulting in an inflated measured velocity. ( C ) Stacks of 2D heatmaps of average number of tracks per filament within each movie frame (left) and average number of tracks per filament in complete movie (right) under various conditions. ( D ) Example of the benefit of “Maximum Track Selection” (MTS) analysis of SAMY movies featuring 10 filaments per movie, moving at velocities ranging from 0.1 to 8 μm/s. Without MTS enabled (−MTS), the number of detected tracks increases with velocity, in spite of a constant number of filaments per frame. With MTS (+MTS), the number of tracks is consistent with the number of filaments and insensitive to velocity. Error bars denote standard deviation.
Article Snippet: Consequently, approaches to automating actin filament motion analysis exist in the form of commercial (e.g., Imaris (Oxford Instruments, Abingdon, UK), Aivia (Leica microsystems, Deerfield, IL), and DiaTrack ( )) as well as custom solutions developed by academic groups ( , , , , , ).
Techniques: Selection, Standard Deviation