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Characterization of the canine immunoglobulin heavy chain repertoire by next generation sequencing

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F18%3A00106638" target="_blank" >RIV/00216224:14740/18:00106638 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.vetimm.2018.07.002" target="_blank" >http://dx.doi.org/10.1016/j.vetimm.2018.07.002</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.vetimm.2018.07.002" target="_blank" >10.1016/j.vetimm.2018.07.002</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Characterization of the canine immunoglobulin heavy chain repertoire by next generation sequencing

  • Original language description

    The ability to mount adaptive immune responses to a diverse array of pathogens is essential to maintaining the health of an individual. The outcome of adaptive immune responses is influenced by the pool of available lymphocyte antigen receptors. Understanding the composition and dynamics of immune repertoires is hence of relevance to characterizing physiologic immunological processes as well as understanding disease pathogenesis. The dog is increasingly recognized as a model for human disease. The objective of this study was to utilize NGS for comprehensive and unbiased analysis of the IGH repertoire in healthy dogs. First, the IGH locus was searched in silico for previously unidentified genes. Second, IGH transcripts from major lymphoid organs were amplified using a 5'RACE approach without V/J primer bias. Third, amplicons were sequenced on an Illumine MiSeq platform, and data were analyzed using the ARResT/Interrogate platform. Data analysis included V/J usage, V-J pairing biases, isotype frequency, CDR3 diversity, convergent recombination, and public repertoires. The results of this study provide a comprehensive IGH repertoire analysis for healthy dogs. These data will allow further improvement of V/J gene-specific primer sets and will serve as baseline for future studies investigating immune repertoires in health and disease.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30102 - Immunology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

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

    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY

  • ISSN

    0165-2427

  • e-ISSN

  • Volume of the periodical

    202

  • Issue of the periodical within the volume

    AUG

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    181-190

  • UT code for WoS article

    000442189700024

  • EID of the result in the Scopus database

    2-s2.0-85050262691