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Validation of a simple low-cost method to monitor ctDNA in patients with solid cancers

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F26475821%3A_____%2F15%3A%230000214" target="_blank" >RIV/26475821:_____/15:#0000214 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=69dded53-c3d6-4118-9ac3-bd909db6632c&cKey=9e0bf2e1-f96e-4102-ba2a-83a65a14c435&mKey=" target="_blank" >http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=69dded53-c3d6-4118-9ac3-bd909db6632c&cKey=9e0bf2e1-f96e-4102-ba2a-83a65a14c435&mKey=</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Validation of a simple low-cost method to monitor ctDNA in patients with solid cancers

  • Original language description

    Poster describing ctDNA monitoring. Detection of circulation tumor DNA (ctDNA) in plasma has become a viable option for non-invasive monitoring of patients. Also termed ,,liquid biopsy? the approach is applicable for pre-diction of response and prediction of resistance to biological therapy (1, 2). Various techniques have been used for ctDNA detection, frequently employing clonal amplification on a digital PCR format (3) with limits of detection (LOD) below 0.01% of mutant alleles. However, these techniques suffer from high complexity, expensive instrumentation, and a considerable cost per sample. We hereby present a simple low-cost alternative that is implementable to routine ctDNA testing. DCE is a simple technique applicable for detection of ctDNA in cancer patients without a need for costly hardware/software equipment. The detection rates are 10 - 15% lower compared to the dedicated dPCR techniques,however, the method requires ca 100x less input DNA, the cost per patient is about 1

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT14383" target="_blank" >NT14383: Use of cfDNA as a new intention for minimally-invasive diagnosis and precise molecular classification of colorectal tumors.</a><br>

  • Continuities

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

Others

  • Publication year

    2015

  • Confidentiality

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