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Development of a technique for the reconstruction and validation of gene network models based on gene expression profiles

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13440%2F18%3A43893642" target="_blank" >RIV/44555601:13440/18:43893642 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.15587/1729-4061.2018.123634" target="_blank" >http://dx.doi.org/10.15587/1729-4061.2018.123634</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.15587/1729-4061.2018.123634" target="_blank" >10.15587/1729-4061.2018.123634</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Development of a technique for the reconstruction and validation of gene network models based on gene expression profiles

  • Original language description

    We have developed a technique for the reconstruction and validation of models of gene networks based on the gene expression profiles derived in the course of DNA microchip experiments or by the method of RNA molecules sequencing. A structural block diagram is presented of a stepwise process for determining optimal parameters of the algorithm for reconstruction of a gene network that meet the optimum network topology. We proposed a comprehensive estimation criterion of a gene network topology based on the Harrington desirability function that contains network topological parameters as constituent components. The maximum value of this criterion corresponds to the optimal topology of a gene network. A technique for the validation of models of gene networks is based on a ROC analysis whose implementation implies a comparative analysis of the character of relations between relevant genes in the network on the basis of the totality of genes and gene networks based on the obtained biclusters. Qualitative reconstruction of a gene network makes it possible to explore the nature of interaction between genes that determine the process of functioning of a biological organism at different stages of development of complex genetic diseases for the purpose of early diagnosis and correction of a given process. It was established that the gene network reconstructed based on the correlation output algorithm is more efficient in comparison with the gene network based on the algorithm ARACNE. The weighted average of relative validation criterion for the derived models based on the correlation output algorithm is significantly greater than the corresponding value when applying the algorithm of ARACNE. This fact indicates a higher degree of compliance with the character of relations between respective genes in the network based on the totality of genes and in the networks based on gene expression profiles in the obtained biclusters. Qualitative reconstruction of a gene network makes it possible to explore the character of development of a biological organism at the gene level, which creates preconditions for early diagnosis and adjustment of the development of different types of genetic diseases.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    10201 - Computer sciences, information science, bioinformathics (hardware development to be 2.2, social aspect to be 5.8)

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Eastern-European Journal of Enterprise Technologies

  • ISSN

    1729-3774

  • e-ISSN

  • Volume of the periodical

    2018

  • Issue of the periodical within the volume

    1/4 (91)

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    19-32

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-85042799438