Some minimization problems for the free analogue of the Fisher information

We consider the free non-commutative analogue Phi^*, introduced by D. Voiculescu, of the concept of Fisher information for random variables. We determine the minimal possible value of Phi^*(a,a^*), if a is a non-commutative random variable subject to the constraint that the distribution of aa^* is prescribed. More generally, we obtain the minimal possible value of Phi^*({a_{ij},a_{ij}^*), if {a_{ij}} is a family of non-commutative random variables such that the distribution of AA^* is prescribed, where A is the matrix (a_{ij}). The d*d-generalization is obtained from the case d=1 via a result of independent interest, concerning the minimal value of Phi^*({a_{ij},a_{ij}^*), when the matrix A=(a_{ij}) and its adjoint have a given joint distribution. We then show how the minimization results obtained for Phi^* lead to maximization results concerning the free entropy chi^*, also defined by Voiculescu.Comment: 31 pages, Late

Random matrix theory for CPA: Generalization of Wegner's nn--orbital model

We introduce a generalization of Wegner's $n$-orbital model for the description of randomly disordered systems by replacing his ensemble of Gaussian random matrices by an ensemble of randomly rotated matrices. We calculate the one- and two-particle Green's functions and the conductivity exactly in the limit $n\to\infty$. Our solution solves the CPA-equation of the $(n=1)$-Anderson model for arbitrarily distributed disorder. We show how the Lloyd model is included in our model.Comment: 3 pages, Rev-Te

Seven-fluorochrome mouse M-FISH for high-resolution analysis of interchromosomal rearrangements

The mouse has evolved to be the primary mammalian genetic model organism. Important applications include the modeling of human cancer and cloning experiments. In both settings, a detailed analysis of the mouse genome is essential. Multicolor karyotyping technologies have emerged to be invaluable tools for the identification of mouse chromosomes and for the deciphering of complex rearrangements. With the increasing use of these multicolor technologies resolution limits are critical. However, the traditionally used probe sets, which employ 5 different fluorochromes, have significant limitations. Here, we introduce an improved labeling strategy. Using 7 fluorochromes we increased the sensitivity for the detection of small interchromosomal rearrangements (700 kb or less) to virtually 100%. Our approach should be important to unravel small interchromosomal rearrangements in mouse models for DNA repair defects and chromosomal instability. Copyright (C) 2003 S. Karger AG, Basel

Mapping of Multiple DNA Gains and Losses in Primary Small Cell Lung Carcinomas by Comparative Genomic Hybridization

Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepresentation of genetic material in 13 autoptic small cell lung cancer specimens. The most abundant genetic changes include DNA losses of chromosome arms 3p, 5q, 10q, 13q, and 17p and DNA gains of 3q, 5p, 8q, and 17q. Amplification sites in these tumors were mapped to 22 chromosome bands. The most frequently involved band was 19q13.1 (4 cases). Bands 1p32, 2p23, 7q11.2, 8q24, and 13q33–34 were involved in two cases each

Chromosomal Gains and Losses in Uveal Melanomas Detected by Comparative Genomic Hybridization

Eleven uveal melanomas were analyzed using comparative genomic hybridization (CGH). The most abundant genetic changes were loss of chromosome 3, overrepresentation of 6p, loss of 6q, and multiplication of 8q. The smallest overrepresented regions on 6p and 8q were 6pterp21 and 8q24qter, respectively. Several additional gains and losses of chromosome segments were repeatedly observed, the most frequent one being loss of 9p (three cases). Monosomy 3 appeared to be a marker for ciliary body involvement. CGH data were compared with the results of chromosome banding. Some alterations, e.g., gains of 6p and losses of 6q, were observed with higher frequencies after CGH, while others, e.g., 9p deletions, were detected only by CGH. The data suggest some similarities of cytogenetic alterations between cutaneous and uveal melanoma. In particular, the 9p deletions are of interest due to recent reports about the location of a putative tumor-suppressor gene for cutaneous malignant melanoma in this region