Cancer Classification with Deep Learning using Genomics Data

Show simple item record

dc.contributor.author Ahsan, Ahmad Omar
dc.contributor.author Ansar, Md. Azmaeen Bin
dc.contributor.author Minhaj, Minhajul Islam
dc.date.accessioned 2022-03-28T06:06:20Z
dc.date.available 2022-03-28T06:06:20Z
dc.date.issued 2021-03-30
dc.identifier.citation [1] Claudio R Alarcón et al. “N 6-methyladenosine marks primary microRNAs for processing”. In: Nature 519.7544 (2015), pp. 482–485. [2] George Adrian Calin et al. “Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia”. In: Proceedings of the national academy of sciences 99.24 (2002), pp. 15524–15529. [3] Jordan M Cummins et al. “The colorectal microRNAome”. In: Proceedings of the National Academy of Sciences 103.10 (2006), pp. 3687–3692. [4] Terrance DeVries and Graham W Taylor. “Dataset augmentation in feature space”. In: arXiv preprint arXiv:1702.05538 (2017). [5] E Melo Felipe De Sousa et al. “Poor-prognosis colon cancer is defined by a molecularly distinct subtype and develops from serrated precursor lesions”. In: Nature medicine 19.5 (2013), pp. 614–618. [6] Douglas Hanahan and Robert A Weinberg. “Hallmarks of cancer: the next generation”. In: cell 144.5 (2011), pp. 646–674. [7] Yoji Hayashita et al. “A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation”. In: Cancer research 65.21 (2005), pp. 9628–9632. [8] JR Jass. “Classification of colorectal cancer based on correlation of clinical, morphological and molecular features”. In: Histopathology 50.1 (2007), pp. 113–130. [9] Jun Lu et al. “MicroRNA expression profiles classify human cancers”. In: nature 435.7043 (2005), pp. 834–838. [10] Xiaoya Luo et al. “MicroRNA signatures: novel biomarker for colorectal cancer?” In: Cancer Epidemiology and Prevention Biomarkers 20.7 (2011), pp. 1272–1286. [11] Brian W Matthews. “Comparison of the predicted and observed secondary structure of T4 phage lysozyme”. In: Biochimica et Biophysica Acta (BBA)-Protein Structure 405.2 (1975), pp. 442–451. [12] Konstantinos J Mavrakis et al. “Genome-wide RNA-mediated interference screen identifies miR-19 targets in Notch-induced T-cell acute lymphoblastic leukaemia”. In: Nature cell biology 12.4 (2010), pp. 372–379. [13] Ali Muhamed Ali et al. “A machine learning approach for the classification of kidney cancer subtypes using mirna genome data”. In: Applied Sciences 8.12 (2018), p. 2422. [14] Ann L Oberg et al. “miRNA expression in colon polyps provides evidence for a multihit model of colon cancer”. In: PloS one 6.6 (2011), e20465. [15] Yong Peng and Carlo M Croce. “The role of MicroRNAs in human cancer”. In: Signal transduction and targeted therapy 1.1 (2016), pp. 1–9. [16] Aaron J Schetter et al. “MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma”. In: Jama 299.4 (2008), pp. 425–436. [17] Aaron J Schetter, Hirokazu Okayama, and Curtis C Harris. “The role of microRNAs in colorectal cancer”. In: Cancer journal (Sudbury, Mass.) 18.3 (2012), p. 244. [18] Mary Shapcott, Katherine J Hewitt, and Nasir Rajpoot. “Deep Learning With Sampling in Colon Cancer Histology”. In: Frontiers in Bioengineering and Biotechnology 7 (2019), p. 52. 42 [19] Yingshuai Sun et al. “Identification of 12 cancer types through genome deep learning”. In: Scientific reports 9.1 (2019), pp. 1–9. [20] H Tagawa and M Seto. “A microRNA cluster as a target of genomic amplification in malignant lymphoma”. In: Leukemia 19.11 (2005), pp. 2013–2016. [21] Justin L Wang et al. “Classification of white blood cells with patternnet-fused ensemble of convolutional neural networks (pecnn)”. In: 2018 IEEE International Symposium on Signal Processing and Information Technology (ISSPIT). IEEE. 2018, pp. 325–330. [22] Wei Yang, Kuanquan Wang, and Wangmeng Zuo. “Neighborhood Component Feature Selection for High-Dimensional Data.” In: JCP 7.1 (2012), pp. 161–168. [23] Lin Zhang et al. “microRNAs exhibit high frequency genomic alterations in human cancer”. In: Proceedings of the National Academy of Sciences 103.24 (2006), pp. 9136–9141. en_US
dc.identifier.uri http://hdl.handle.net/123456789/1294
dc.description Supervised by Mr. Tareque Mohmud Chowdhury, Assistant Professor, Co-supervisor Mr. Tasnim Ahmed Lecturer, Department of CSE, Islamic University of Technology, Gazipur, Bangladesh. en_US
dc.description.abstract Deep learning has been monumental in Computer Vision, Natural Language Processing, Machine Translation task and so on. In bioinformatics, Deep learning is playing an important role in drug discover and protein structure prediction. In cancer diagnosis, thanks to advances in Computer Vision Deep Learning models are able to accurately classify cancer. However, not much work has been done in the field of Cancer diagnosis with genomic data. Several authors attempted to use genomic data using machine learning, however it was restricted to single cancer subtypes. In this thesis, we explored classification of all types of cancer using miRNA genome data by creating new model architectures. We are proposing two new architectures a basic ANN and a novel architecture based on ResNet called CResNet. We have trained 4 different kinds of model. LSTM, Artificial Neural Network, CResNet (Variant of ResNet Architecture) and Ensemble models using model averaging. Our models have achieved MCC (Mathew’s correlation coefficient) value of 0.8596,0.9625,0.9745 and 0.9439 which is greater than the SOTA model’s MCC model demonstrating that our architecture performed better than the current architecture. en_US
dc.language.iso en en_US
dc.publisher Department of Computer Science and Engineering (CSE), Islamic University of Technology (IUT), Board Bazar, Gazipur-1704, Bangladesh en_US
dc.title Cancer Classification with Deep Learning using Genomics Data en_US
dc.type Thesis en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search IUT Repository


Advanced Search

Browse

My Account

Statistics