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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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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