Publications by authors named "Alistair Forbes"

Article Synopsis
  • Photometric stereo is a technique that uses images taken from different lighting angles to create 3D models of objects, which can help engineers assess and monitor damage on surfaces like concrete.
  • A dataset was created combining real measurements from 9 different objects and synthetic data from 12 virtual models, allowing for a thorough comparison of results and uncertainties in the measurements.
  • This dataset can be utilized to enhance photometric stereo methods, improve uncertainty quantification for monitoring structural health in concrete, and develop better data processing techniques for aligning varied test results.
View Article and Find Full Text PDF

A novel method to double the measurement range of wavelength scanning interferometery (WSI) is described. In WSI the measured optical path difference (OPD) is affected by a sign ambiguity, that is, from an interference signal it is not possible to distinguish whether the OPD is positive or negative. The sign ambiguity can be resolved by measuring an interference signal in quadrature.

View Article and Find Full Text PDF

A method to obtain unambiguous surface height measurements using wavelength scanning interferometry with an improved repeatability, comparable to that obtainable using phase shifting interferometry, is reported. Rather than determining the conventional fringe frequency-derived z height directly, the method uses the frequency to resolve the fringe order ambiguity, and combine this information with the more accurate and repeatable fringe phase derived z height. A theoretical model to evaluate the method's performance in the presence of additive noise is derived and shown to be in good agreement with experiments.

View Article and Find Full Text PDF

The aim of precision engineering is the accurate control of geometry. For this reason, mathematics has a long association with precision engineering: from the calculation and correction of angular scales used in surveying and astronomical instrumentation to statistical averaging techniques used to increase precision. This study illustrates the enabling role the mathematical sciences are playing in precision engineering: modelling physical processes, instruments and complex geometries, statistical characterization of metrology systems and error compensation.

View Article and Find Full Text PDF

In this paper, we describe techniques for extracting features from surface topography data, gathered by a 3D-microscopy system, on a length scale that is relevant for cell attachment. The feature parameters considered include standard surface roughness parameters applied to the complete surface as well as new feature parameters designed to quantify local variations in surface topography potentially influencing cell behaviour. Methodologies have been developed both to determine the degree of homogeneity or isotropy of a surface and to compare the topographies of different samples.

View Article and Find Full Text PDF
Article Synopsis
  • Copy number variants (CNVs) are significant in human genetic diversity and may influence susceptibility to common diseases.
  • A study analyzed around 19,000 individuals for associations between CNVs and eight common diseases using a specialized array that covered many polymorphic CNVs.
  • The findings indicated that while some CNV loci were linked to diseases, they largely overlap with previously identified single nucleotide polymorphisms (SNPs), suggesting that common CNVs may not play a major role in the genetic underpinnings of these diseases.
View Article and Find Full Text PDF

Crohn's disease (CD) and ulcerative colitis (UC) have a strong genetic component, contributing to a patient's susceptibility for inflammatory bowl disease (IBD). Linkage analysis has detected an IBD susceptibility locus in a region on chromosome 7q that encompasses the p47 (NCF1) gene and p47 (PsiNCF1) pseudogenes. Involvement of the NCF1 locus in IBD was supported by the observation that chronic inflammation of the bowel is a feature of chronic granulomatous disease caused by NCF1 mutation in 25% of cases.

View Article and Find Full Text PDF