We discuss status of the minimal supersymmetric SO(10) in both low and split supersymmetry regime. To demonstrate viability of the model we present a good fit of the fermion masses and their mixings. The solution needs a strongly split supersymmetry with gauginos and higgsinos around 102 TeV, sfermions close to 1014 GeV and a GUT scale of around 6×1015 GeV. It predicts fast proton decay rates, hierarchical neutrino masses and large leptonic mixing angle sinθ13≈0.1.

Spatial correspondence between histology and multi sequence MRI can provide information about the capabilities of non-invasive imaging to characterize cancerous tissue. However, shrinkage and deformation occurring during the excision of the tumor and the histological processing complicate the co registration of MR images with histological sections. This work proposes a methodology to establish a detailed 3D relation between histology sections and in vivo MRI tumor data. The key features of the methodology are a very dense histological sampling (up to 100 histology slices per tumor), mutual information based non-rigid B-spline registration, the utilization of the whole 3D data sets, and the exploitation of an intermediate ex vivo MRI. In this proof of concept paper, the methodology was applied to one tumor. We found that, after registration, the visual alignment of tumor borders and internal structures was fairly accurate. Utilizing the intermediate ex vivo MRI, it was possible to account for changes caused by the excision of the tumor: we observed a tumor expansion of 20%. Also the effects of fixation, dehydration and histological sectioning could be determined: 26% shrinkage of the tumor was found. The annotation of viable tissue, performed in histology and transformed to the in vivo MRI, matched clearly with high intensity regions in MRI. With this methodology, histological annotation can be directly related to the corresponding in vivo MRI. This is a vital step for the evaluation of the feasibility of multi-spectral MRI to depict histological groundtruth.

Understanding and efficiently representing skills is one of the most important problems in a general Programming by Demonstration (PbD) paradigm. We present Growing Hierarchical Dynamic Bayesian Networks (GHDBN), an adaptive variant of the general DBN model able to learn and to represent complex skills. The structure of the model, in terms of number of states and possible transitions between them, is not needed to be known a priori. Learning in the model is performed incrementally and in an unsupervised manner.

Background:In search of a proposed viral aetiology of childhood acute lymphoblastic leukaemia (ALL), the common species C adenoviruses were analysed in Guthrie cards.Methods:Guthrie cards from 243 children who later developed ALL and from 486 matched controls were collected and analysed by nested polymerase chain reaction for the presence of adenovirus DNA.Results:Adenovirus DNA was reliably detected from only two subjects, both of whom developed ALL.Conclusion:Adenovirus DNA is detected in Guthrie card samples at too low a frequency to reveal an association between adenovirus and the development of leukaemia.