Deep learning-based polyp segmentation network with a dual encoder-decoder

dc.contributor.authorLewis, John
dc.contributor.examiningcommitteeWu, Nan (Mechanical Engineering)en_US
dc.contributor.examiningcommitteeFiorillo, Graziano (Civil Engineering)en_US
dc.contributor.supervisorCha, Young-Jin
dc.date.accessioned2022-08-12T14:02:14Z
dc.date.available2022-08-12T14:02:14Z
dc.date.copyright2022-08-11
dc.date.issued2022-08-11
dc.date.submitted2022-08-11T21:55:02Zen_US
dc.degree.disciplineCivil Engineeringen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractColorectal cancer (CRC) constitutes one of the most serious forms of cancers across the world. Current screening procedures through imaging with colonoscopy are costly, laborious, and time consuming. Computer-aided diagnosis (CAD) and the integration of deep learning within the field have provided the opportunity for improvements with respect to human error. The recent developments with convolutional neural networks (CNNs) have demonstrated the capacity for real time detection and semantic segmentation of early signs of CRC. These early signs of CRC are referred to as polyps, and thus the identification of these potentially cancerous tumors improves patient outcomes and mortality rates associated with CRC. In an effort to compensate for some of the issues presented for current screening procedures, a novel polyp segmentation network, PSNet [1], is proposed for the semantic segmentation of polyps. PSNet compensates for current issues affecting polyp segmentation networks such as boundary pixel definitions, as well as model generalization and overfitting issues. PSNet provides state-of-the-art (SOTA) performance with respect to two major semantic segmentation performance metrics, mean intersection-over-union (mIoU) and mean Dice (mDice) on 5 major publicly available datasets, with a combined mIoU and mDice score of 0.863 and 0.797 across all sets, respectively. A new configuration of these 5 publicly available datasets is also proposed to improve upon model generalization and help demonstrate some of the issues associated with current standards of polyp datasets and performance evaluation. The mIoU and mDice score for this new configured dataset was 0.941 and 0.897, respectively, and therefore improved even further on the reported SOTA results.en_US
dc.description.noteOctober 2022en_US
dc.description.sponsorshipFunder: Canadian Foundation for Innovation (CFI) Award title: John R. Evans Leaders Fund (JELF) Award Number: 37394 Award URL: https://www.innovation.ca/apply-manage-awards/funding-opportunities/john-r-evans-leaders-funden_US
dc.identifier.urihttp://hdl.handle.net/1993/36673
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectdeep learningen_US
dc.subjectconvolutional neural networksen_US
dc.subjectpolypsen_US
dc.subjectsegmentationen_US
dc.subjecttransformersen_US
dc.titleDeep learning-based polyp segmentation network with a dual encoder-decoderen_US
dc.typemaster thesisen_US
local.subject.manitobanoen_US
oaire.awardNumber4914en_US
oaire.awardTitleInnovation Proof-of-Concept Granten_US
oaire.awardURIhttps://researchmanitoba.ca/funding-opportunities/innovation-proof-of-concept-grant/en_US
project.funder.identifierhttp://dx.doi.org/10.13039/100008794en_US
project.funder.nameResearch Manitobaen_US
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