Pith. sign in

REVIEW

Autofocusing technologies for whole slide imaging and automated microscopy

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2006.08610 v2 pith:MCU4QLY6 submitted 2020-06-15 physics.med-ph eess.IVphysics.optics

classification physics.med-pheess.IVphysics.optics
keywords focusapproachesautofocusingautomatedimagingmicroscopytraditionalaccurate
verification ladder T0 review T1 audit T2 compute T3 formal
0 comments
read the original abstract

Whole slide imaging (WSI) has moved digital pathology closer to diagnostic practice in recent years. Due to the inherent tissue topography variability, accurate autofocusing remains a critical challenge for WSI and automated microscopy systems. The traditional focus map surveying method is limited in its ability to acquire a high degree of focus points while still maintaining high throughput. Real-time approaches decouple image acquisition from focusing, thus allowing for rapid scanning while maintaining continuous accurate focus. This work reviews the traditional focus map approach and discusses the choice of focus measure for focal plane determination. It also discusses various real-time autofocusing approaches including reflective-based triangulation, confocal pinhole detection, low-coherence interferometry, tilted sensor approach, independent dual sensor scanning, beam splitter array, phase detection, dual-LED illumination, and deep-learning approaches. The technical concepts, merits, and limitations of these methods are explained and compared to those of a traditional WSI system. This review may provide new insights for the development of high-throughput automated microscopy imaging systems that can be made broadly available and utilizable without loss of capacity.

Discussion (0). Continue with ORCID to comment.

Pith tools