Histopathological Image QTL Discovery of Immune Infiltration Variants
Joseph D. Barry,
Maud Fagny,
Joseph N. Paulson,
Hugo J.W.L. Aerts,
John Platig,
John Quackenbush
Affiliations
Joseph D. Barry
Center for Cancer Computational Biology and Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 667 Huntington Avenue, Boston, MA 02115, USA; Corresponding author
Maud Fagny
Center for Cancer Computational Biology and Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 667 Huntington Avenue, Boston, MA 02115, USA
Joseph N. Paulson
Center for Cancer Computational Biology and Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 667 Huntington Avenue, Boston, MA 02115, USA
Hugo J.W.L. Aerts
Department of Radiology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA
John Platig
Center for Cancer Computational Biology and Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 667 Huntington Avenue, Boston, MA 02115, USA
John Quackenbush
Center for Cancer Computational Biology and Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 667 Huntington Avenue, Boston, MA 02115, USA
Summary: Genotype-to-phenotype association studies typically use macroscopic physiological measurements or molecular readouts as quantitative traits. There are comparatively few suitable quantitative traits available between cell and tissue length scales, a limitation that hinders our ability to identify variants affecting phenotype at many clinically informative levels. Here we show that quantitative image features, automatically extracted from histopathological imaging data, can be used for image quantitative trait loci (iQTLs) mapping and variant discovery. Using thyroid pathology images, clinical metadata, and genomics data from the Genotype-Tissue Expression (GTEx) project, we establish and validate a quantitative imaging biomarker for immune cell infiltration. A total of 100,215 variants were selected for iQTL profiling and tested for genotype-phenotype associations with our quantitative imaging biomarker. Significant associations were found in HDAC9 and TXNDC5. We validated the TXNDC5 association using GTEx cis-expression QTL data and an independent hypothyroidism dataset from the Electronic Medical Records and Genomics network. : Pathology; Bioinformatics; Computational Bioinformatics; Association Analysis Subject Areas: Pathology, Bioinformatics, Computational Bioinformatics, Association Analysis