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An image-to-answer algorithm for fully automated digital PCR image processing

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F22%3APU145666" target="_blank" >RIV/00216305:26620/22:PU145666 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064165:_____/22:10442785 RIV/00216208:11110/22:10442785

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2022/LC/D1LC01175H" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2022/LC/D1LC01175H</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d1lc01175h" target="_blank" >10.1039/d1lc01175h</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    An image-to-answer algorithm for fully automated digital PCR image processing

  • Original language description

    The digital polymerase chain reaction (dPCR) is an irreplaceable variant of PCR techniques due to its capacity for absolute quantification and detection of rare deoxyribonucleic acid (DNA) sequences in clinical samples. Image processing methods, including micro-chamber positioning and fluorescence analysis, determine the reliability of the dPCR results. However, typical methods demand high requirements for the chip structure, chip filling, and light intensity uniformity. This research developed an image-to-answer algorithm with single fluorescence image capture and known image-related error removal. We applied the Hough transform to identify partitions in the images of dPCR chips, the 2D Fourier transform to rotate the image, and the 3D projection transformation to locate and correct the positions of all partitions. We then calculated each partition's average fluorescence amplitudes and generated a 3D fluorescence intensity distribution map of the image. We subsequently corrected the fluorescence non-uniformity between partitions based on the map and achieved statistical results of partition fluorescence intensities. We validated the proposed algorithms using different contents of the target DNA. The proposed algorithm is independent of the dPCR chip structure damage and light intensity non-uniformity. It also provides a reliable alternative to analyze the results of chip-based dPCR systems.

  • 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

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/LTACH19005" target="_blank" >LTACH19005: High Precision Digital PCR for cfDNA Detection in Noninvasive Prenatal Testing (NIPT) Applications</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    LAB ON A CHIP

  • ISSN

    1473-0197

  • e-ISSN

    1473-0189

  • Volume of the periodical

    22

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    1333-1343

  • UT code for WoS article

    000765868800001

  • EID of the result in the Scopus database

    2-s2.0-85124137073