In the post-genomics era, an emphasis has been placed on disentangling 'genotype-phenotype' 3 connections so that the biological basis of complex phenotypes can be understood. However, 4 our ability to efficiently and comprehensively characterize phenotypes lags behind our ability to 5 characterize genomes. Here, we report a toolbox for fast and reproducible high-throughput 6 dense phenotyping of 3D images. Given a target image, a rigid registration is first used to orient 7 a template to the target surface, then the template is transformed further to fit the specific shape 8 of the target using a non-rigid transformation model. As validation, we used N = 41 3D facial 9images registered with MeshMonk and manually landmarked at 19 locations. We demonstrate 10 that the MeshMonk registration is accurate, with 0.62 mm as the average root mean squared 11 error between the manual and automatic placements and no variation in landmark position or 12 centroid size significantly attributable to landmarking method used. Though validated using 19 13 landmarks for comparison with traditional methods, MeshMonk allows for automatic dense 14phenotyping, thus facilitating more comprehensive investigations of 3D shape variation. This 15 expansion opens up an exciting avenue of study in assessing genomic and phenomic data to 16better understand the genetic contributions to complex morphological traits.
18 19The phenotypic complement to genomics is phenomics, which aims to obtain high-throughput 20and high-dimensional phenotyping in line with our ability to characterize genomes 1 . The 21 paradigm shift is simple and similar to the one made in the Human Genome Project: instead of 22'phenotyping as usual' or measuring a limited set of simplified features that seem relevant, why 23 not measure it all? In contrast to genomic technologies, which successfully measure and 24 characterize complete genomes, the scientific development of phenomics lags behind. 25However, with the advent of new technologies, hardware exists for extensively and intensively 26collecting quantitative phenotypic data. For example, 3D image surface and/or medical 27 scanners provide the optimal means to capture information of biological morphology and 28appearance. Today, the challenge is to establish standardized and comprehensive phenotypic 29representations from large scale image data that can be used to study phenotypic variation in 30 the context of genetic variation 2 . This is a challenge that we address with the development of 31the MeshMonk toolbox, which enables fast and reproducible high-throughput phenotyping of 3D 32images, or quasi-landmark indication, which can be applied to 3D facial images as well as 3D 33scans of other complex morphological structures.
35Dense correspondence phenotyping is important beyond genomics and could be employed by 36anthropologists, biologists, and medical clinicians to accurately and reproducibly characterize 37anatomical structures such that underlying qualities about the structure can be understood. The 38 study of va...