Robust hierarchical density estimation and regression for re-stained histological whole slide image co-registration

• Published in: PloS one 2019-07, Vol.14 (7), p.e0220074-e0220074
• Main Authors: Jiang, Jun, Larson, Nicholas B, Prodduturi, Naresh, Flotte, Thomas J, Hart, Steven N
• Format: Article
• Language: English
• Subjects: Analysis; Benchmarking; Biology and Life Sciences; Cell density; Computer applications; Density; Digital imaging; EDTA; Eosin; Fluoresceins; Fluorescent Antibody Technique - methods; Hematoxylin; Histology; Identification methods; Image Processing, Computer-Assisted - methods; Image registration; Immunohistochemistry; Medical imaging; Medicine and Health Sciences; Methods; Pathology; Physical Sciences; Proteins; Registration; Regression analysis; Research and Analysis Methods; Robustness (mathematics); Staining and Labeling - methods; Stains & staining
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0220074

For many disease conditions, tissue samples are colored with multiple dyes and stains to add contrast and location information for specific proteins to accurately identify and diagnose disease. This presents a computational challenge for digital pathology, as whole-slide images (WSIs) need to be properly overlaid (i.e. registered) to identify co-localized features. Traditional image registration methods sometimes fail due to the high variation of cell density and insufficient texture information in WSIs-particularly at high magnifications. In this paper, we proposed a robust image registration strategy to align re-stained WSIs precisely and efficiently. This method is applied to 30 pairs of immunohistochemical (IHC) stains and their hematoxylin and eosin (H&E) counterparts. Our approach advances the existing methods in three key ways. First, we introduce refinements to existing image registration methods. Second, we present an effective weighting strategy using kernel density estimation to mitigate registration errors. Third, we account for the linear relationship across WSI levels to improve accuracy. Our experiments show significant decreases in registration errors when matching IHC and H&E pairs, enabling subcellular-level analysis on stained and re-stained histological images. We also provide a tool to allow users to develop their own registration benchmarking experiments.