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Rapid automated landmarking for morphometric analysis of three-dimensional facial scans.
Li, Mao; Cole, Joanne B; Manyama, Mange; Larson, Jacinda R; Liberton, Denise K; Riccardi, Sheri L; Ferrara, Tracey M; Santorico, Stephanie A; Bannister, Jordan J; Forkert, Nils D; Spritz, Richard A; Mio, Washington; Hallgrimsson, Benedikt.
Affiliation
  • Li M; Department of Mathematics, Florida State University, Tallahassee, FL, USA.
  • Cole JB; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, CO, USA.
  • Manyama M; Department of Anatomy, Catholic University of Health and Allied Sciences, Mwanza, Tanzania.
  • Larson JR; Department of Anatomy and Cell Biology, McCaig Institute for Bone and Joint Health, and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada.
  • Liberton DK; National Institutes of Health (NIDCR), Bethesda, MD, USA.
  • Riccardi SL; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, CO, USA.
  • Ferrara TM; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, CO, USA.
  • Santorico SA; Department of Mathematical and Statistical Science, University of Colorado Denver, Denver, CO, USA.
  • Bannister JJ; Department of Radiology and Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.
  • Forkert ND; Department of Radiology and Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.
  • Spritz RA; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, CO, USA.
  • Mio W; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
  • Hallgrimsson B; Department of Mathematics, Florida State University, Tallahassee, FL, USA.
J Anat ; 230(4): 607-618, 2017 Apr.
Article in En | MEDLINE | ID: mdl-28078731
Automated phenotyping is essential for the creation of large, highly standardized datasets from anatomical imaging data. Such datasets can support large-scale studies of complex traits or clinical studies related to precision medicine or clinical trials. We have developed a method that generates three-dimensional landmark data that meet the requirements of standard geometric morphometric analyses. The method is robust and can be implemented without high-performance computing resources. We validated the method using both direct comparison to manual landmarking on the same individuals and also analyses of the variation patterns and outlier patterns in a large dataset of automated and manual landmark data. Direct comparison of manual and automated landmarks reveals that automated landmark data are less variable, but more highly integrated and reproducible. Automated data produce covariation structure that closely resembles that of manual landmarks. We further find that while our method does produce some landmarking errors, they tend to be readily detectable and can be fixed by adjusting parameters used in the registration and control-point steps. Data generated using the method described here have been successfully used to study the genomic architecture of facial shape in two different genome-wide association studies of facial shape.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Imaging, Three-Dimensional / Face / Genome-Wide Association Study / Biometric Identification Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: J Anat Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Imaging, Three-Dimensional / Face / Genome-Wide Association Study / Biometric Identification Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: J Anat Year: 2017 Type: Article Affiliation country: United States