(English) The dissertation explores the vowel system of Czech L3 Spanish, focusing on three facets of its architecture: vowel quality (following SLM by Flege 1995, 1999, 2003), vowel quantity and vocalic sequences between words. Preliminary studies (Čechová 2013, 2014) suggest that there might be some evidence for the Mechanism of Equivalence in Czech L3 Spanish, since the vowel spaces of both languages consist of the same categories, with different phonetic realizations. Hence, the more similar the sounds are, the harder it is to capture the relevant difference, necessary to attain native-like pronunciation. Vowel quantity, being traditionally associated with the phonological feature of length in Czech (Palková 1994), is not present in Spanish, and compensating for that property, some Czech speakers tend to pronounce accented syllables with extraordinarily longer durations. Finally, vowel sequences in Spanish are usually subjetct to resyllabification, whereas Czech prefers glottalization to keep morphemes of words separated. These predictions were tested in 22 university Czech students with advanced level of Spanish (C1-C1). Subsequent analysis revealed consistent inclination towards L1 in terms of vowel quality, in less extent in vowel quantity, and although the prevalecent strategy for majority...

Modification of DNA sequences and their suitable representation is important part of analysis, comparison and another processing. Goal of this paper is finding of suitable methods for representation of genomic and proteomic sequences. Because there is great number of metods, this paper will introduce only some of them. All selected methods, are described in the first part of this paper and they were programed in Matlab. Selected methods are illustrated on coding sequences of the first exon of the b-globin gene of 11 different species. Results are compared withresults from the original papers. Some methods are capable of another processing like cluster analysis. Output of this paper is comparison of results, gained from different methods, and finding the most suitable one.

This thesis discusses about possibilities of construction colour DNA spectrograms and about patterns which can be detected there. Spectrograms as tools of spectral analysis give us a simultaneous view of the local frequency throughout the nucleotide sequence. They are suitable for gene identification or gene regions identification, determination of global character about whole chromosomes and also give us a chance for the discovery of yet unknown regions of potential significance. For purpose of this kind of DNA analysis is possible to use digital signal processing methods. We can apply them on only after conversion of DNA sequence to numerical representation. Selection of correct numerical representation affects how well will be reflected biological features in numerical record which we need for another use in digital signal analysis.

T1 mapping of myocardial tissue is important for diagnostics of myocardial fibrosis. Cardiac magnetic resonance imaging of small animals is challenging due to high heart and respiratory rates. Pulse sequences for T1 mapping are proposed in this thesis based on inversion recovery FLASH and Intragate FLASH. The sequence IR FLASH was compared to the reference sequence RARE on a static phantom. Both sequences were applied for measuring the myocardium of a rat. For T1 quantification a software in Matlab was developed. Using this software, T1 maps of rat myocardium were calculated.

This paper deals with the effect of the MR pulse sequences on the temperature of the measured object. The theoretical part is dedicated to basic principle of magnetic resonance, the selected pulse sequences and risks that are connected with MRI. There is also described the draft of the testing phantom and information about the measurement and record of temperature during MR measurement. In the experimental part the effect of RF coils, pulse sequences and parameters of pulse sequences are tested on drafted phantom with experimental MR device located at the Institut of Scientific Instruments of the AS CR in Brno. These findings are then tested on live laboratory mouse. All results are analyzed and used as default data for developed simulation program.

This diploma thesis deals with the DCE – MRI method (Dynamic contrast enhanced magnetic resonance imaging). Basic principle of magnetic resonance and pulse sequence is described. The diploma thesis focuses on the DCE method, especially on the description of the processing procedure by this method. Description of selected pharmacokinetic models is the part of this diploma thesis as well. Furthermore, description and realization of batch processing by PerfLab system is presented. For verifying purposes of the batch processing functionality real data were measured using created acquisition protocol, which is also part of the diploma thesis.

Mobile genetic elements are occupied by this project. It is aimed at their features, which can be used for their detection. It also deals with issue of conversion of symbolic sequence into numerical form. Classifications of mobile genetic elements are explained, basic types of mobile genetic sequences are described, and principles of numerical maps and detection in symbolic represetation are also clarified. Conversion of symbolic genetical sequences by chosen numerical map and calculation of normalized correlation values for set of mobile genetic elements are compiled. Analysis of the mobile genetic elements properties is performed for design of detector. The library of themes is created at the end for usage by designed detector.

The specific recognition of the DNA is crucial for the correct functioning of the cell. Although its mechanisms are extensively studied, the actual process is not yet fully understood, partly due to the variance observed in readout mechanisms so far. In this work, a particular type of specific recognition is examined: the shape readout in the DNA minor groove. Based on a sta- tistical analysis of three-dimensional structures of protein-DNA complexes acquired from the Protein Data Bank, I propose a previously unrecorded readout mechanism of widened minor grooves by hydrophobic amino acids. In addition, the effect of DNA sequence on the topography of the contacted locus, the preferred secondary structures and the interaction between the protein and DNA are explored, as well as the relative information amount of examined features concerning the DNA deformation. 1

Burkholderia cenocepcia is one of the serious infectious agents of respiratory tract among cystic fibrosis patients. There are problems mainly with strains which are capable of epidemic spread. The known epidemic in the Czech Republic was caused by ST32 strain in the past. In this work, there was completed whole genome sequence of referential isolate 1232 of B. cenocepacia ST32 in cooperation with bioinformatics by new generation sequencing techniques and by determining the problematic areas by a combination of Sanger sequencing bioinformatics approaches and manual assembling of sequence reads localized in these areas. The final version of the genome sequence was annotated by PGAAP and at the present time it is finalized. Second part of this work is dedicated to looking for a prognostic marker of infection caused by ST32 strain in patients with cystic fibrosis. We analysed the results of ST32 trancriptomic experiment and chose genes possibly connected with the cepacia syndrome - serious, mostly fatal state of infection. By quantitative PCR we compared their expression in isolates from 4 patients from time of cepacia syndrome and month before that. We checked the possibility of direct detection of the expression of these genes in clinical material. We identified genes for type III secretion system as...

Melampyrum nemorosum agg. is very complicated group of hemiparasitic plants. According to the traditional concept, 15 species is distinguished. Recent molecular analyses show a need of critical taxonomic revision of group and a potential importance of ancient hybridization. Analysis of 3 regions of cpDNA (trnTUGU-trnLUAA, psbA-trnHGUG, rpl32-trnLUAG) and 2 regions of nuclear DNA (Agt1 and At103) reveals well supported lineage with limited geographical distribution. Morphology and genome size of genetically supported lineages were compared.