dc.identifier.citation |
[1] Hyuna Sung et al. “Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries”. In: CA: a cancer journal for clinicians 71.3 (2021), pp. 209–249. [2] Kristen Trost Mantlo. “Understanding Young Adult Survivors of Childhood Cancers’ Participation in Late Effects Screening: A Mixed Methods Approach”. PhD thesis. Old Dominion University, 2019. [3] David A Hanauer et al. “Bioinformatics approaches in the study of cancer”. In: Current molecular medicine 7.1 (2007), pp. 133–141. [4] Yi-Ping Phoebe Chen and Feng Chen. “Identifying targets for drug discovery using bioinformatics”. In: Expert opinion on therapeutic targets 12.4 (2008), pp. 383–389. [5] Jun Wang et al. “Regulatory roles of long noncoding RNAs implicated in cancer hallmarks”. In: International journal of cancer 146.4 (2020), pp. 906–916. [6] Aisha Patel. “Benign vs malignant tumors”. In: JAMA oncology 6.9 (2020), pp. 1488–1488. [7] David V Schapira et al. “Intensive care, survival, and expense of treating criti cally III cancer patients”. In: Jama 269.6 (1993), pp. 783–786. [8] Julie Eggert. “Genetics and genomics in oncology nursing: what does every nurse need to know?” In: Nursing Clinics 52.1 (2017), pp. 1–25. [9] Ying Lu and Jiawei Han. “Cancer classification using gene expression data”. In: Information Systems 28.4 (2003), pp. 243–268. [10] Kirk J Mantione et al. “Comparing bioinformatic gene expression profiling methods: microarray and RNA-Seq”. In: Medical science monitor basic re search 20 (2014), p. 138. 78 REFERENCES 79 [11] Matthew E Ritchie et al. “limma powers differential expression analyses for RNA-sequencing and microarray studies”. In: Nucleic acids research 43.7 (2015), e47–e47. [12] Christine H Chung, Philip S Bernard, and Charles M Perou. “Molecular por traits and the family tree of cancer”. In: Nature genetics 32.4 (2002), pp. 533– 540. [13] Douglas Hanahan and Robert A Weinberg. “Hallmarks of cancer: the next gen eration”. In: cell 144.5 (2011), pp. 646–674. [14] Andre Esteva et al. “Dermatologist-level classification of skin cancer with deep neural networks”. In: nature 542.7639 (2017), pp. 115–118. [15] E Farshi. “Peptide-Based mRNA Vaccines”. In: J Gastro Hepato 9.16 (2023), pp. 1–6. [16] Davide Ruggero and Pier Paolo Pandolfi. “Does the ribosome translate cancer?” In: Nature Reviews Cancer 3.3 (2003), pp. 179–192. [17] Wengong Si et al. “The role and mechanisms of action of microRNAs in cancer drug resistance”. In: Clinical epigenetics 11.1 (2019), pp. 1–24. [18] Edward L Tatum. “Molecular biology, nucleic acids, and the future of medicine”. In: Perspectives in biology and medicine 10.1 (1966), pp. 19–32. [19] Lela Buckingham. “Fundamentals of Nucleic Acid Biochemistry: An Overview”. In: (). [20] Francis Crick. “Central dogma of molecular biology”. In: Nature 227.5258 (1970), pp. 561–563. [21] Robert G Roeder. “Transcriptional regulation and the role of diverse coactiva tors in animal cells”. In: FEBS letters 579.4 (2005), pp. 909–915. [22] Melissa J Moore. “From birth to death: the complex lives of eukaryotic mR NAs”. In: Science 309.5740 (2005), pp. 1514–1518. [23] Richard W Carthew and Erik J Sontheimer. “Origins and mechanisms of miR NAs and siRNAs”. In: Cell 136.4 (2009), pp. 642–655. REFERENCES 80 [24] David P Bartel. “MicroRNAs: genomics, biogenesis, mechanism, and func tion”. In: cell 116.2 (2004), pp. 281–297. [25] John L Rinn and Howard Y Chang. “Genome regulation by long noncoding RNAs”. In: Annual review of biochemistry 81 (2012), pp. 145–166. [26] Timothy H Bestor. “The DNA methyltransferases of mammals”. In: Human molecular genetics 9.16 (2000), pp. 2395–2402. [27] M Perou Charles et al. “Molecular portraits of human breast tumours”. In: Na ture 406.6797 (2000), pp. 747–752. [28] Gyongyi Munk ¨ acsy, Libero Santarpia, and Bal ´ azs Gy ´ orffy. “Gene Expression ˝ Profiling in Early Breast Cancer—Patient Stratification Based on Molecular and Tumor Microenvironment Features”. In: Biomedicines 10.2 (2022), p. 248. [29] George A Calin and Carlo M Croce. “MicroRNA signatures in human cancers”. In: Nature reviews cancer 6.11 (2006), pp. 857–866. [30] Barbara Pardini et al. “Noncoding RNAs in extracellular fluids as cancer biomark ers: the new frontier of liquid biopsies”. In: Cancers 11.8 (2019), p. 1170. [31] Hui Li et al. “A neoplastic gene fusion mimics trans-splicing of RNAs in normal human cells”. In: Science 321.5894 (2008), pp. 1357–1361. [32] Kenzui Taniue and Nobuyoshi Akimitsu. “Fusion genes and RNAs in cancer development”. In: Non-coding RNA 7.1 (2021), p. 10. [33] Konstantina Kourou et al. “Machine learning applications in cancer progno sis and prediction”. In: Computational and structural biotechnology journal 13 (2015), pp. 8–17. [34] Meriem Amrane et al. “Breast cancer classification using machine learning”. In: 2018 electric electronics, computer science, biomedical engineerings’ meeting (EBBT). IEEE. 2018, pp. 1–4. REFERENCES 81 [35] Sara Tarek, Reda Abd Elwahab, and Mahmoud Shoman. “Gene expression based cancer classification”. In: Egyptian Informatics Journal 18.3 (2017), pp. 151– 159. ISSN: 1110-8665. DOI: https://doi.org/10.1016/j.eij.2016.12. 001. URL: https://www.sciencedirect.com/science/article/pii/ S1110866516300809. [36] Maxim D Podolsky et al. “Evaluation of machine learning algorithm utilization for lung cancer classification based on gene expression levels”. In: Asian Pacific journal of cancer prevention 17.2 (2016), pp. 835–838. [37] Boyu Lyu and Anamul Haque. “Deep learning based tumor type classification using gene expression data”. In: Proceedings of the 2018 ACM international conference on bioinformatics, computational biology, and health informatics. 2018, pp. 89–96. [38] Joseph M de Guia, Madhavi Devaraj, and Carson K Leung. “DeepGx: deep learning using gene expression for cancer classification”. In: Proceedings of the 2019 IEEE/ACM International Conference on Advances in Social Networks Analysis and Mining. 2019, pp. 913–920. [39] Yuanyuan Li et al. “A comprehensive genomic pan-cancer classification us ing The Cancer Genome Atlas gene expression data”. In: BMC genomics 18.1 (2017), pp. 1–13. [40] Pradipta Maji and Chandra Das. “Relevant and significant supervised gene clus ters for microarray cancer classification”. In: IEEE Transactions on nanobio science 11.2 (2012), pp. 161–168. [41] Yi-Hsin Hsu and Dong Si. “Cancer type prediction and classification based on rna-sequencing data”. In: 2018 40th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE. 2018, pp. 5374–5377. [42] Milad Mostavi et al. “Convolutional neural network models for cancer type prediction based on gene expression”. In: BMC medical genomics 13 (2020), pp. 1–13. REFERENCES 82 [43] Jean-Franc¸ois Laplante and Moulay A Akhloufi. “Predicting cancer types from miRNA stem-loops using deep learning”. In: 2020 42nd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE. 2020, pp. 5312–5315. [44] Kazi Ferdous Mahin et al. “PanClassif: Improving pan cancer classification of single cell RNA-seq gene expression data using machine learning”. In: Ge nomics 114.2 (2022), p. 110264. [45] Leo Breiman. “Random forests”. In: Machine learning 45.1 (2001), pp. 5–32. [46] Yoav Freund, Robert Schapire, and Naoki Abe. “A short introduction to boost ing”. In: Journal-Japanese Society For Artificial Intelligence 14.771-780 (1999), p. 1612. [47] Anestis Antoniadis, Sophie Lambert-Lacroix, and Fred´ erique Leblanc. “Effec- ´ tive dimension reduction methods for tumor classification using gene expres sion data”. In: Bioinformatics 19.5 (2003), pp. 563–570. [48] D Pavithra and B Lakshmanan. “Feature selection and classification in gene expression cancer data”. In: 2017 International Conference on Computational Intelligence in Data Science (ICCIDS). IEEE. 2017, pp. 1–6. [49] Yongjun Piao and Keun Ho Ryu. “Detection of differentially expressed genes using feature selection approach from RNA-seq”. In: 2017 IEEE International Conference on Big Data and Smart Computing (BigComp). IEEE. 2017, pp. 304– 308. [50] Hanaa Salem, Gamal Attiya, and Nawal El-Fishawy. “Classification of human cancer diseases by gene expression profiles”. In: Applied Soft Computing 50 (2017), pp. 124–134. [51] Isabelle Guyon et al. “Gene selection for cancer classification using support vector machines”. In: Machine learning 46.1 (2002), pp. 389–422. [52] Alejandro Lopez-Rincon et al. “Automatic discovery of 100-miRNA signature for cancer classification using ensemble feature selection”. In: BMC bioinfor matics 20.1 (2019), pp. 1–17. REFERENCES 83 [53] Pilar Garcıa-Dıaz et al. “Unsupervised feature selection algorithm for multiclass cancer classification of gene expression RNA-Seq data”. In: Genomics 112.2 (2020), pp. 1916–1925. [54] Yu-Heng Lai et al. “Overall survival prediction of non-small cell lung cancer by integrating microarray and clinical data with deep learning”. In: Scientific reports 10.1 (2020), p. 4679. [55] Dejun Zhang et al. “Integrating feature selection and feature extraction methods with deep learning to predict clinical outcome of breast cancer”. In: Ieee Access 6 (2018), pp. 28936–28944. [56] JN Weinstein. “TCGAR Network, EA Collisson et al.,“The cancer genome at las pan-cancer analysis project,”” in: Nature Genetics 45.10 (2013), pp. 1113– 1120. [57] Yingdong Zhao et al. “TPM, FPKM, or normalized counts? A comparative study of quantification measures for the analysis of RNA-seq data from the NCI patient-derived models repository”. In: Journal of translational medicine 19.1 (2021), pp. 1–15. [58] Cole Trapnell et al. “Transcript assembly and quantification by RNA-Seq re veals unannotated transcripts and isoform switching during cell differentiation”. In: Nature biotechnology 28.5 (2010), pp. 511–515. [59] Bo Li and Colin N Dewey. “RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome”. In: BMC bioinformatics 12 (2011), pp. 1–16. [60] Mia Huljanah et al. “Feature selection using random forest classifier for pre dicting prostate cancer”. In: IOP Conference Series: Materials Science and En gineering. Vol. 546. 5. IOP Publishing. 2019, p. 052031. [61] David G Kleinbaum et al. Logistic regression. Springer, 2002. [62] Lipo Wang. Support vector machines: theory and applications. Vol. 177. Springer Science & Business Media, 2005. REFERENCES 84 [63] Tianqi Chen and Carlos Guestrin. “Xgboost: A scalable tree boosting system”. In: Proceedings of the 22nd acm sigkdd international conference on knowledge discovery and data mining. 2016, pp. 785–794. [64] Daniel Svozil, Vladimir Kvasnicka, and Jiri Pospichal. “Introduction to multi layer feed-forward neural networks”. In: Chemometrics and intelligent labora tory systems 39.1 (1997), pp. 43–62. [65] Serkan Kiranyaz et al. “1D convolutional neural networks and applications: A survey”. In: Mechanical systems and signal processing 151 (2021), p. 107398. [66] Ravisutha Sakrepatna Srinivasamurthy. “Understanding 1D Convolutional Neu ral Networks Using Multiclass Time-Varying Signalss”. PhD thesis. Clemson University, 2018. [67] Sercan O Arik and Tomas Pfister. “Tabnet: Attentive interpretable tabular learn- ¨ ing”. In: Proceedings of the AAAI Conference on Artificial Intelligence. Vol. 35. 8. 2021, pp. 6679–6687. [68] Hans Hersbach. “Decomposition of the continuous ranked probability score for ensemble prediction systems”. In: Weather and Forecasting 15.5 (2000), pp. 559–570. [69] Robi Polikar. “Ensemble based systems in decision making”. In: IEEE Circuits and systems magazine 6.3 (2006), pp. 21–45. [70] Scott M Lundberg and Su-In Lee. “A unified approach to interpreting model predictions”. In: Advances in neural information processing systems 30 (2017). [71] Hao Luo et al. “DEG 15, an update of the Database of Essential Genes that in cludes built-in analysis tools”. In: Nucleic acids research 49.D1 (2021), pp. D677– D686. [72] Michael I Love, Wolfgang Huber, and Simon Anders. “Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2”. In: Genome biology 15.12 (2014), pp. 1–21. REFERENCES 85 [73] Sanjaya K Panda, Subhrajit Nag, and Prasanta K Jana. “A smoothing based task scheduling algorithm for heterogeneous multi-cloud environment”. In: 2014 In ternational Conference on Parallel, Distributed and Grid Computing. IEEE. 2014, pp. 62–67. [74] SGOPAL Patro and Kishore Kumar Sahu. “Normalization: A preprocessing stage”. In: arXiv preprint arXiv:1503.06462 (2015). [75] C Saranya and G Manikandan. “A study on normalization techniques for pri vacy preserving data mining”. In: International Journal of Engineering and Technology (IJET) 5.3 (2013), pp. 2701–2704. [76] Md Manjurul Ahsan et al. “Effect of data scaling methods on machine learning algorithms and model performance”. In: Technologies 9.3 (2021), p. 52. [77] Ekaba Bisong and Ekaba Bisong. “Introduction to Scikit-learn”. In: Building Machine Learning and Deep Learning Models on Google Cloud Platform: A Comprehensive Guide for Beginners (2019), pp. 215–229. [78] VN Ganapathi Raju et al. “Study the influence of normalization/transformation process on the accuracy of supervised classification”. In: 2020 Third Interna tional Conference on Smart Systems and Inventive Technology (ICSSIT). IEEE. 2020, pp. 729–735. [79] Zaneta Swiderska-Chadaj et al. “Impact of rescanning and normalization on convolutional neural network performance in multi-center, whole-slide classifi cation of prostate cancer”. In: Scientific Reports 10.1 (2020), pp. 1–14. [80] Junfang Wu and Chao Li. “Feature selection based on features unit”. In: 2017 4th International Conference on Information Science and Control Engineering (ICISCE). IEEE. 2017, pp. 330–333. [81] Huiqing Liu, Jinyan Li, and Limsoon Wong. “A comparative study on feature selection and classification methods using gene expression profiles and pro teomic patterns”. In: Genome informatics 13 (2002), pp. 51–60. REFERENCES 86 [82] Zena M Hira and Duncan F Gillies. “A review of feature selection and feature extraction methods applied on microarray data”. In: Advances in bioinformatics 2015 (2015). [83] Valeria Fonti and Eduard Belitser. “Feature selection using lasso”. In: VU Ams terdam research paper in business analytics 30 (2017), pp. 1–25. [84] Jason Brownlee. “An introduction to feature selection”. In: Machine learning process 6 (2014). [85] R Muthukrishnan and R Rohini. “LASSO: A feature selection technique in pre dictive modeling for machine learning”. In: 2016 IEEE international conference on advances in computer applications (ICACA). IEEE. 2016, pp. 18–20. [86] Anamika Chauhan et al. “Detection of lung cancer using machine learning tech niques based on routine blood indices”. In: 2020 IEEE international conference for innovation in technology (INOCON). IEEE. 2020, pp. 1–6. [87] Hui Zou and Trevor Hastie. “Regression shrinkage and selection via the elastic net, with applications to microarrays”. In: JR Stat Soc Ser B 67 (2003), pp. 301– 20. [88] Asma Agaal and Mansour Essgaer. “Influence of Feature Selection Methods on Breast Cancer Early Prediction Phase using Classification and Regression Tree”. In: 2022 International Conference on Engineering & MIS (ICEMIS). IEEE. 2022, pp. 1–6. [89] Robert Tibshirani. “Regression shrinkage and selection via the lasso”. In: Jour nal of the Royal Statistical Society: Series B (Methodological) 58.1 (1996), pp. 267–288. [90] Fabian Pedregosa et al. “Scikit-learn: Machine learning in Python”. In: the Jour nal of machine Learning research 12 (2011), pp. 2825–2830. [91] Jerome Friedman, Trevor Hastie, and Rob Tibshirani. “Regularization paths for generalized linear models via coordinate descent”. In: Journal of statistical soft ware 33.1 (2010), p. 1. REFERENCES 87 [92] Artem Sokolov et al. “Pathway-based genomics prediction using generalized elastic net”. In: PLoS computational biology 12.3 (2016), e1004790. [93] Amrita Basu et al. “RWEN: response-weighted elastic net for prediction of chemosensitivity of cancer cell lines”. In: Bioinformatics 34.19 (2018), pp. 3332– 3339. [94] Mahmood Khalsan et al. “A survey of machine learning approaches applied to gene expression analysis for cancer prediction”. In: IEEE Access 10 (2022), pp. 27522–27534. [95] Jose Linares-Blanco, Alejandro Pazos, and Carlos Fernandez-Lozano. “Ma- ˜ chine learning analysis of TCGA cancer data”. In: PeerJ Computer Science 7 (2021), e584. [96] Ahsan Bin Tufail et al. “Deep learning in cancer diagnosis and prognosis pre diction: a minireview on challenges, recent trends, and future directions”. In: Computational and Mathematical Methods in Medicine 2021 (2021). [97] Vabiyana Safira Desdhanty and Zuherman Rustam. “Liver cancer classification using random forest and extreme gradient boosting (xgboost) with genetic algo rithm as feature selection”. In: 2021 International Conference on Decision Aid Sciences and Application (DASA). IEEE. 2021, pp. 716–719. [98] Bong-Hyun Kim, Kijin Yu, and Peter CW Lee. “Cancer classification of single cell gene expression data by neural network”. In: Bioinformatics 36.5 (2020), pp. 1360–1366. [99] Sk Md Mosaddek Hossain et al. “Pan-cancer classification by regularized multi task learning”. In: Scientific reports 11.1 (2021), p. 24252. [100] Yulin Zhang et al. “A novel XGBoost method to identify cancer tissue-of origin based on copy number variations”. In: Frontiers in genetics 11 (2020), p. 585029. [101] Jerome H Friedman. “Stochastic gradient boosting”. In: Computational statis tics & data analysis 38.4 (2002), pp. 367–378. REFERENCES 88 [102] Xiaobo Zhou, Kuang-Yu Liu, and Stephen TC Wong. “Cancer classification and prediction using logistic regression with Bayesian gene selection”. In: Journal of Biomedical Informatics 37.4 (2004), pp. 249–259. [103] Zakariya Yahya Algamal and Muhammad Hisyam Lee. “Penalized logistic re gression with the adaptive LASSO for gene selection in high-dimensional can cer classification”. In: Expert Systems with Applications 42.23 (2015), pp. 9326– 9332. [104] Zakariya Yahya Algamal and Muhammad Hisyam Lee. “Regularized logistic regression with adjusted adaptive elastic net for gene selection in high dimen sional cancer classification”. In: Computers in biology and medicine 67 (2015), pp. 136–145. [105] Lingyun Gao et al. “Hybrid method based on information gain and support vector machine for gene selection in cancer classification”. In: Genomics, pro teomics & bioinformatics 15.6 (2017), pp. 389–395. [106] Ahmed Arafa et al. “Regularized logistic regression model for cancer classifica tion”. In: 2021 38th National Radio Science Conference (NRSC). Vol. 1. IEEE. 2021, pp. 251–261. [107] Trevor Hastie. “Ridge regularization: An essential concept in data science”. In: Technometrics 62.4 (2020), pp. 426–433. [108] Enrique Alba et al. “Gene selection in cancer classification using PSO/SVM and GA/SVM hybrid algorithms”. In: 2007 IEEE congress on evolutionary compu tation. IEEE. 2007, pp. 284–290. [109] Mikel Galar et al. “An overview of ensemble methods for binary classifiers in multi-class problems: Experimental study on one-vs-one and one-vs-all schemes”. In: Pattern Recognition 44.8 (2011), pp. 1761–1776. [110] Luıs A Vale Silva and Karl Rohr. “Pan-cancer prognosis prediction using multi modal deep learning”. In: 2020 IEEE 17th International Symposium on Biomed ical Imaging (ISBI). IEEE. 2020, pp. 568–571. REFERENCES 89 [111] Niousha Bagheri Khoulenjani et al. “Cancer miRNA biomarkers classification using a new representation algorithm and evolutionary deep learning”. In: Soft Computing 25 (2021), pp. 3113–3129. [112] Thomas Serre, Aude Oliva, and Tomaso Poggio. “A feedforward architecture accounts for rapid categorization”. In: Proceedings of the national academy of sciences 104.15 (2007), pp. 6424–6429. [113] U Ravindran and C Gunavathi. “A survey on gene expression data analysis using deep learning methods for cancer diagnosis”. In: Progress in Biophysics and Molecular Biology 177 (2023), pp. 1–13. [114] Pablo Guillen and Jerry Ebalunode. “Cancer classification based on microarray gene expression data using deep learning”. In: 2016 International Conference on Computational Science and Computational Intelligence (CSCI). IEEE. 2016, pp. 1403–1405. [115] Feng Gao et al. “DeepCC: a novel deep learning-based framework for cancer molecular subtype classification”. In: Oncogenesis 8.9 (2019), p. 44. [116] Bing Xu et al. “Empirical evaluation of rectified activations in convolutional network”. In: arXiv preprint arXiv:1505.00853 (2015). [117] Diederik P Kingma and Jimmy Ba. “Adam: A method for stochastic optimiza tion”. In: arXiv preprint arXiv:1412.6980 (2014). [118] Mohanad Mohammed et al. “A stacking ensemble deep learning approach to cancer type classification based on TCGA data”. In: Scientific reports 11.1 (2021), pp. 1–22. [119] Sergey Ioffe and Christian Szegedy. “Batch normalization: Accelerating deep network training by reducing internal covariate shift”. In: International confer ence on machine learning. pmlr. 2015, pp. 448–456. [120] Nitish Srivastava et al. “Dropout: a simple way to prevent neural networks from overfitting”. In: The journal of machine learning research 15.1 (2014), pp. 1929–1958. REFERENCES 90 [121] Jimmy Lei Ba, Jamie Ryan Kiros, and Geoffrey E Hinton. “Layer normaliza tion”. In: arXiv preprint arXiv:1607.06450 (2016). [122] Madhuri Gokhale, Sraban Kumar Mohanty, and Aparajita Ojha. “GeneViT: Gene vision transformer with improved DeepInsight for cancer classification”. In: Computers in Biology and Medicine 155 (2023), p. 106643. [123] Anwar Khan and Boreom Lee. “Gene transformer: Transformers for the gene expression-based classification of lung cancer subtypes”. In: arXiv preprint arXiv:2108.11833 (2021). [124] Ting-He Zhang et al. “Transformer for Gene Expression Modeling (T-GEM): An Interpretable Deep Learning Model for Gene Expression-Based Phenotype Predictions”. In: Cancers 14.19 (2022), p. 4763. [125] Faysal Bin Rahman, Farhan Anjum, and Musaddiq Hasan Fatin Khan. “Detec tion of Lung Adenocarcinoma Cancer based on RNA-seq gene expression data using LIMMA and TabNet”. PhD thesis. Department of Computer Science and Engineering (CSE), Islamic University of . . ., 2022. [126] R Tyler McLaughlin et al. “Fast, accurate, and racially unbiased pan-cancer tumor-only variant calling with tabular machine learning”. In: NPJ Precision Oncology 7.1 (2023), p. 4. [127] Ahmad Nasimian et al. “A deep tabular data learning model predicting cisplatin sensitivity identifies BCL2L1 dependency in cancer”. In: Computational and Structural Biotechnology Journal (2023). [128] Yawen Xiao et al. “A deep learning-based multi-model ensemble method for cancer prediction”. In: Computer methods and programs in biomedicine 153 (2018), pp. 1–9. [129] Aik Choon Tan and David Gilbert. “Ensemble machine learning on gene ex pression data for cancer classification”. In: (2003). [130] Eloise Withnell et al. “XOmiVAE: an interpretable deep learning model for can cer classification using high-dimensional omics data”. In: Briefings in Bioinfor matics 22.6 (2021), bbab315. REFERENCES 91 [131] Scott M Lundberg and Su-In Lee. “A Unified Approach to Interpreting Model Predictions”. In: Advances in Neural Information Processing Systems 30. Ed. by I. Guyon et al. Curran Associates, Inc., 2017, pp. 4765–4774. URL: http:// papers.nips.cc/paper/7062-a-unified-approach-to-interpreting model-predictions.pdf. [132] Wilson E Marcılio and Danilo M Eler. “From explanations to feature selection: assessing SHAP values as feature selection mechanism”. In: 2020 33rd SIB GRAPI conference on Graphics, Patterns and Images (SIBGRAPI). Ieee. 2020, pp. 340–347. [133] Masrur Sobhan and Ananda Mohan Mondal. “Explainable Machine Learning to Identify Patient-specific Biomarkers for Lung Cancer”. In: 2022 IEEE Inter national Conference on Bioinformatics and Biomedicine (BIBM). IEEE. 2022, pp. 3152–3159. [134] Katsuya Futagami et al. “Pairwise acquisition prediction with SHAP value in terpretation”. In: The Journal of Finance and Data Science 7 (2021), pp. 22– 44. [135] Melvyn Yap et al. “Verifying explainability of a deep learning tissue classifier trained on RNA-seq data”. In: Scientific reports 11.1 (2021), p. 2641. [136] Michael Chromik. “Making SHAP Rap: Bridging local and global insights through interaction and narratives”. In: Human-Computer Interaction–INTERACT 2021: 18th IFIP TC 13 International Conference, Bari, Italy, August 30–September 3, 2021, Proceedings, Part II 18. Springer. 2021, pp. 641–651. [137] A Stupnikov et al. “Robustness of differential gene expression analysis of RNA seq”. In: Computational and structural biotechnology journal 19 (2021), pp. 3470– 3481. [138] Adam McDermaid et al. “Interpretation of differential gene expression results of RNA-seq data: review and integration”. In: Briefings in bioinformatics 20.6 (2019), pp. 2044–2054. [139] Qingguo Wang et al. “Enabling cross-study analysis of RNA-Sequencing data”. In: BioRxiv (2017), p. 110734. [140] Qingguo Wang et al. “Unifying cancer and normal RNA sequencing data from different sources”. In: Scientific data 5.1 (2018), pp. 1–8. [141] Nick Bunkley. “Joseph Juran, Pioneer in Quality Control, Dies”. In: The New York Times 103 (2008). [142] V Roshan Joseph. “Optimal ratio for data splitting”. In: Statistical Analysis and Data Mining: The ASA Data Science Journal 15.4 (2022), pp. 531–538. [143] Denny Wu and Ji Xu. “On the Optimal Weighted ℓ2 Regularization in Overpa rameterized Linear Regression”. In: Advances in Neural Information Process ing Systems 33 (2020), pp. 10112–10123. |
en_US |