Machine Learning for Genomics and Therapeutics Resources

This repo accompanies our survey paper:

Machine Learning Applications for Therapeutic Tasks with Genomics Data. Kexin Huang, Cao Xiao, Lucas M. Glass, Cathy W. Critchlow, Greg Gibson, Jimeng Sun Published in Patterns.

We list tools, algorithms, data for this area. Feel free to make a pull request for new resources.

Machine Learning for Genomics and Therapeutics Resources

Machine Learning for Genomics in Target Discovery

Theme 1: Facilitating Understanding of Human Biology

Task 1: DNA-protein and RNA-protein binding prediction

Task Description Given a set of DNA/RNA sequences predict their binding scores. After training,use feature importance attribution methods to identify the motifs.

Jian Zhou and Olga G Troyanskaya. Predicting effects of noncoding variants with deep learning–based sequence model. Nature Methods, 12(10):931–934, 2015.

Babak Alipanahi, Andrew Delong, Matthew T Weirauch, and Brendan J Frey. Predicting the sequence specificities of dna-and rna-binding proteins by deep learning. Nature Biotechnology, 33(8):831–838, 2015.

Martin Kircher, Daniela M Witten, Preti Jain, Brian J O’Roak, Gregory M Cooper, and Jay Shendure. A general framework for estimating the relative pathogenicity of human genetic variants. Nature Genetics, 46(3):310–315, 2014.

David R Kelley, Jasper Snoek, and John L Rinn. Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks. Genome Research, 26(7):990–999, 2016.

Qinhu Zhang, Lin Zhu, and De-Shuang Huang. High-order convolutional neural network architecture for predicting dna-protein binding sites. IEEE/ACM transactions on Computational Biology and Bioinformatics, 16(4):1184–1192, 2018.

Zhen Cao and Shihua Zhang. Simple tricks of convolutional neural network architectures improve dna–protein binding prediction. Bioinformatics, 35(11):1837–1843, 2019.

Task 2: Methylation state prediction

Task Description For a DNA/RNA position with missing methylation status, given its availableneighboring methylation states and the DNA/RNA sequence, predict the methylation status on the positionof interest.

Keith D Robertson. Dna methylation and human disease. Nature Reviews Genetics, 6(8):597–610, 2005.

Weiwei Zhang, Tim D Spector, Panos Deloukas, Jordana T Bell, and Barbara E Engelhardt. Predicting genome-wide dna methylation using methylation marks, genomic position, and dna regulatory elements. Genome Biology, 16(1):1–20, 2015.

John W Whitaker, Zhao Chen, and Wei Wang. Predicting the human epigenome from dna motifs. Nature Methods, 12(3):265, 2015.

Chantriolnt-Andreas Kapourani and Guido Sanguinetti. Melissa: Bayesian clustering and imputation of single-cell methylomes. Genome Biology, 20(1):1–15, 2019.

Joshua J Levy, Alexander J Titus, Curtis L Petersen, Youdinghuan Chen, Lucas A Salas, and Brock C Christensen. Methylnet: an automated and modular deep learning approach for dna methylation analysis. BMC Bioinformatics, 21(1):1–15, 2020.

Quan Zou, Pengwei Xing, Leyi Wei, and Bin Liu. Gene2vec: gene subsequence embedding for prediction of mammalian n6-methyladenosine sites from mrna. RNA, 25(2):205–218, 2019

Task 3: RNA splicing prediction

Task Description Given an RNA sequence and its cell type, if available, for each nucleotide,predicts the probability of being a spliced breakpoint and the splicing level.

Núria López-Bigas, Benjamin Audit, Christos Ouzounis, Genís Parra, and Roderic Guigó. Are splicing mutations the most frequent cause of hereditary disease? FEBS Letters, 579(9):1900–1903, 2005.

Sahar Gelfman, Quanli Wang, K Melodi McSweeney, Zhong Ren, Francesca La Carpia, Matt Halvorsen, Kelly Schoch, Fanni Ratzon, Erin L Heinzen, Michael J Boland, et al. Annotating pathogenic non-coding variants in genic regions. Nature Communications, 8(1):1–11, 2017.

Joseph M Paggi and Gill Bejerano. A sequence-based, deep learning model accurately predicts rna splicing branchpoints. RNA, 24(12):1647–1658, 2018.

Karthik A Jagadeesh, Joseph M Paggi, S Ye James, Peter D Stenson, David N Cooper, Jonathan A Bernstein, and Gill Bejerano. S-cap extends pathogenicity prediction to genetic variants that affect rna splicing. Nature Genetics, 51(4):755–763, 2019.

Task 4: Spatial gene expression inference

Task Description Given the histopathology image of the tissue, predict the gene expression forevery gene at each spatial transcriptomics spot.

Patrik L Ståhl, Fredrik Salmén, Sanja Vickovic, Anna Lundmark, José Fernández Navarro, Jens Magnusson, Stefania Giacomello, Michaela Asp, Jakub O Westholm, Mikael Huss, et al. Visualization and analysis of gene expression in tissue sections by spatial transcriptomics. Science, 353(6294):78–82, 2016.

Alona Levy-Jurgenson, Xavier Tekpli, Vessela N Kristensen, and Zohar Yakhini. Spatial transcriptomics inferred from pathology whole-slide images links tumor heterogeneity to survival in breast and lung cancer. Scientific Reports, 10(1):1–11, 2020.

Task 5: Cell composition analysis

Task Description Given the gene expressions of a set of cells (in bulk RNA-seq or a spot in spatialtranscriptomics), infer proportion estimates of each cell type for this set.

Mikala Egeblad, Elizabeth S Nakasone, and Zena Werb. Tumors as organs: complex tissues that interface with the entire organism. Developmental Cell, 18(6):884–901, 2010.

Francisco Avila Cobos, Jo Vandesompele, Pieter Mestdagh, and Katleen De Preter. Computational deconvolution of transcriptomics data from mixed cell populations. Bioinformatics, 34(11):1969–1979, 2018.

Aaron M Newman, Chih Long Liu, Michael R Green, Andrew J Gentles, Weiguo Feng, Yue Xu, Chuong D Hoang, Maximilian Diehn, and Ash A Alizadeh. Robust enumeration of cell subsets from tissue expression profiles. Nature Methods, 12(5):453–457, 2015.

Kevin Menden, Mohamed Marouf, Sergio Oller, Anupriya Dalmia, Daniel Sumner Magruder, Karin Kloiber, Peter Heutink, and Stefan Bonn. Deep learning–based cell composition analysis from tissue expression profiles. Science Advances, 6(30):eaba2619, 2020.

Alma Andersson, Joseph Bergenstråhle, Michaela Asp, Ludvig Bergenstråhle, Aleksandra Jurek, José Fernández Navarro, and Joakim Lundeberg. Single-cell and spatial transcriptomics enables probabilistic inference of cell type topography. Communications Biology, 3(1):1–8, 2020.

Jing Su and Qianqian Song. Dstg: Deconvoluting spatial transcriptomics data through graph-based artificial intelligence. Briefings in Bioinformatics, 2020.

Task 6: Gene network construction

Task Description Given a set of gene expression profiles of a gene set, identify the gene regulatorynetwork by predicting all pairs of interacting genes.

Anne-Claire Haury, Fantine Mordelet, Paola Vera-Licona, and Jean-Philippe Vert. Tigress: trustful inference of gene regulation using stability selection. BMC Systems Biology, 6(1):1–17, 2012.

Vân Anh Huynh-Thu, Alexandre Irrthum, Louis Wehenkel, and Pierre Geurts. Inferring regulatory networks from expression data using tree-based methods. PloS One, 5(9):1–10, 2010.

Thomas Moerman, Sara Aibar Santos, Carmen Bravo González-Blas, Jaak Simm, Yves Moreau, Jan Aerts, and Stein Aerts. Grnboost2 and arboreto: efficient and scalable inference of gene regulatory networks. Bioinformatics, 35(12):2159–2161, 2019.

Theme 2: Identifying Druggable Biomarkers

Task 1: Variant calling

Task Description Given the aligned sequencing data ((1) read pileup image, which is a matrix ofdimension M and N, with M the number of reads and N the length of reads; or (2) the raw reads, which are aset of sequences strings) for each locus, classify the multi-class variant status.

Ryan Poplin, Pi-Chuan Chang, David Alexander, Scott Schwartz, Thomas Colthurst, Alexander Ku, Dan Newburger, Jojo Dijamco, Nam Nguyen, Pegah T Afshar, et al. A universal snp and small-indel variant caller using deep neural networks. Nature Biotechnology, 36(10):983–987, 2018.

Ruibang Luo, Fritz J Sedlazeck, Tak-Wah Lam, and Michael C Schatz. A multi-task convolutional deep neural network for variant calling in single molecule sequencing. Nature Communications, 10(1):1–11, 2019.

Ruibang Luo, Chak-Lim Wong, Yat-Sing Wong, Chi-Ian Tang, Chi-Man Liu, Chi-Ming Leung, and Tak-Wah Lam. Exploring the limit of using a deep neural network on pileup data for germline variant calling. Nature Machine Intelligence, 2(4):220–227, 2020.

Justin M Zook, Jennifer McDaniel, Nathan D Olson, Justin Wagner, Hemang Parikh, Haynes Heaton, Sean A Irvine, Len Trigg, Rebecca Truty, Cory Y McLean, et al. An open resource for accurately benchmarking small variant and reference calls. Nature Biotechnology, 37(5):561–566, 2019.

Olivier Delaneau, Jean-Francois Zagury, and Jonathan Marchini. Improved whole-chromosome phasing for disease and population genetic studies. Nature Methods, 10(1):5–6, 2013.

Task 2: Variant pathogenicity prioritization

Task Description Given features about a variant, predict its corresponding disease risk and thenrank all variants based on the disease risk. Alternatively, given the DNA sequence or other related genomicsfeatures, predict the likelihood of disease risk for this sequence and retrieve the variant in the sequence thatcontributes highly to the risk prediction.

Daniel Quang, Yifei Chen, and Xiaohui Xie. Dann: a deep learning approach for annotating the pathogenicity of genetic variants. Bioinformatics, 31(5):761–763, 2015.

Charles Kooperberg, Michael LeBlanc, and Valerie Obenchain. Risk prediction using genome-wide association studies. Genetic Epidemiology, 34(7):643–652, 2010.

Guillaume Paré, Shihong Mao, and Wei Q Deng. A machine-learning heuristic to improve gene score prediction of polygenic traits. Scientific Reports, 7(1):1–11, 2017.

Task 3: Rare disease detection

Task Description Given the gene expression data and other auxiliary data of a patient predictwhether this patient has a rare disease. Also, identify genetic variants for this rare disease

Philip J Vickers. Challenges and opportunities in the treatment of rare diseases. Drug Discovery World, 14:9–16, 2013.

Bojian Yin, Marleen Balvert, Rick AA van der Spek, Bas E Dutilh, Sander Bohté, Jan Veldink, and Alexander Schönhuth. Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype. Bioinformatics, 35(14):i538–i547, 2019.

Limeng Cui, Siddharth Biswal, Lucas M Glass, Greg Lever, Jimeng Sun, and Cao Xiao. Conan: Complementary pattern augmentation for rare disease detection. In AAAI, volume 34, pages 614–621, 2020.

Jaclyn N Taroni, Peter C Grayson, Qiwen Hu, Sean Eddy, Matthias Kretzler, Peter A Merkel, and Casey S Greene. Multiplier: a transfer learning framework for transcriptomics reveals systemic features of rare disease. Cell Systems, 8(5):380–394, 2019.

Task 4: Gene-disease association prediction

Task Description Given the known gene-disease association network and auxiliary information,predict the association likelihood for every unknown gene-disease pair.

Cecily J Wolfe, Isaac S Kohane, and Atul J Butte. Systematic survey reveals general applicability of" guilt-by-association" within gene coexpression networks. BMC Bioinformatics, 6(1):1–10, 2005.

Sebastian Köhler, Sebastian Bauer, Denise Horn, and Peter N Robinson. Walking the interactome for prioritization of candidate disease genes. The American Journal of Human Genetics, 82(4):949–958, 2008.

Kexin Huang, Cao Xiao, Lucas M Glass, Marinka Zitnik, and Jimeng Sun. Skipgnn: predicting molecular interactions with skip-graph networks. Scientific Reports, 10(1):1–16, 2020.

Léon-Charles Tranchevent, Amin Ardeshirdavani, Sarah ElShal, Daniel Alcaide, Jan Aerts, Didier Auboeuf, and Yves Moreau. Candidate gene prioritization with endeavour. Nucleic Acids Research, 44(W1):W117–W121, 2016.

Ping Luo, Yuanyuan Li, Li-Ping Tian, and Fang-Xiang Wu. Enhancing the prediction of disease–gene associations with multimodal deep learning. Bioinformatics, 35(19):3735–3742, 2019.

Juan J Cáceres and Alberto Paccanaro. Disease gene prediction for molecularly uncharacterized diseases. PLoS Computational Biology, 15(7):e1007078, 2019.

Task 5: Pathway analysis and prediction

Task Description Given the gene expression data for a phenotype and known gene relations, identify a set of genes corresponding to disease pathways.

Aravind Subramanian, Pablo Tamayo, Vamsi K Mootha, Sayan Mukherjee, Benjamin L Ebert, Michael A Gillette, Amanda Paulovich, Scott L Pomeroy, Todd R Golub, Eric S Lander, et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences, 102(43):15545–15550, 2005.

Adi Laurentiu Tarca, Sorin Draghici, Purvesh Khatri, Sonia S Hassan, Pooja Mittal, Jung-sun Kim, Chong Jai Kim, Juan Pedro Kusanovic, and Roberto Romero. A novel signaling pathway impact analysis. Bioinformatics, 25(1):75–82, 2009.

Ivan V Ozerov, Ksenia V Lezhnina, Evgeny Izumchenko, Artem V Artemov, Sergey Medintsev, Quentin Vanhaelen, Alexander Aliper, Jan Vijg, Andreyan N Osipov, Ivan Labat, et al. In silico pathway activation network decomposition analysis (ipanda) as a method for biomarker development. Nature Communications, 7(1):1–11, 2016.

Matthew A Reyna, David Haan, Marta Paczkowska, Lieven PC Verbeke, Miguel Vazquez, Abdullah Kahraman, Sergio Pulido-Tamayo, Jonathan Barenboim, Lina Wadi, Priyanka Dhingra, et al. Pathway and network analysis of more than 2500 whole cancer genomes. Nature Communications, 11(1):1–17, 2020.

Jonathan R Karr, Jayodita C Sanghvi, Derek N Macklin, Miriam V Gutschow, Jared M Jacobs, Benjamin Bolival Jr, Nacyra Assad-Garcia, John I Glass, and Markus W Covert. A whole-cell computational model predicts phenotype from genotype. Cell, 150(2):389–401, 2012.

Jianzhu Ma, Michael Ku Yu, Samson Fong, Keiichiro Ono, Eric Sage, Barry Demchak, Roded Sharan, and Trey Ideker. Using deep learning to model the hierarchical structure and function of a cell. Nature Methods, 15(4):290, 2018.

Haitham A Elmarakeby, Justin Hwang, David Liu, Saud H AlDubayan, Keyan Salari, Camden Richter, Taylor E Arnoff, Jihye Park, William C Hahn, and Eliezer Van Allen. Biologically informed deep neural network for prostate cancer classification and discovery. bioRxiv, 2020.

Machine Learning for Genomics in Therapeutics Discovery

Theme 1: Improving Context-specific Drug Response

Task 1: Drug Response Prediction

Task Description Given a pair of drug compound molecular structure and gene expression profile of the cell line, predict the drug response in this context

Ladislav Rampášek, Daniel Hidru, Petr Smirnov, Benjamin Haibe-Kains, and Anna Goldenberg. Dr. vae: improving drug response prediction via modeling of drug perturbation effects. Bioinformatics, 35(19):3743–3751, 2019.

Mehmet Tan, Ozan Fırat Özgül, Batuhan Bardak, Işıksu Ekşioğlu, and Suna Sabuncuoğlu. Drug response prediction by ensemble learning and drug-induced gene expression signatures. Genomics, 111(5):1078–1088, 2019.

Naiqian Zhang, Haiyun Wang, Yun Fang, Jun Wang, Xiaoqi Zheng, and X Shirley Liu. Predicting anticancer drug responses using a dual-layer integrated cell line-drug network model. PLoS Computational Biology, 11(9):e1004498, 2015.

Mehreen Ali and Tero Aittokallio. Machine learning and feature selection for drug response prediction in precision oncology applications. Biophysical Reviews, 11(1):31–39, 2019.

Jianzhu Ma, Samson H Fong, Yunan Luo, Christopher J Bakkenist, John Paul Shen, Soufiane Mourragui, Lodewyk FA Wessels, Marc Hafner, Roded Sharan, Jian Peng, et al. Few-shot learning creates predictive models of drug response that translate from high-throughput screens to individual patients. Nature Cancer, pages 1–12, 2021.

Brent M Kuenzi, Jisoo Park, Samson H Fong, Kyle S Sanchez, John Lee, Jason F Kreisberg, Jianzhu Ma, and Trey Ideker. Predicting drug response and synergy using a deep learning model of human cancer cells. Cancer Cell, 38(5):672–684, 2020

Task 2: Drug Combination Therapy Prediction

Task Description Given a combination of drug compound structures and a cell line’s genomics profile, predict the combination response.

Peng Li, Chao Huang, Yingxue Fu, Jinan Wang, Ziyin Wu, Jinlong Ru, Chunli Zheng, Zihu Guo, Xuetong Chen, Wei Zhou, et al. Large-scale exploration and analysis of drug combinations. Bioinformatics, 31(12):2007–2016, 2015.

Jan Wildenhain, Michaela Spitzer, Sonam Dolma, Nick Jarvik, Rachel White, Marcia Roy, Emma Griffiths, David S Bellows, Gerard D Wright, and Mike Tyers. Prediction of synergism from chemical-genetic interactions by machine learning. Cell Systems, 1(6):383–395, 2015.

Kristina Preuer, Richard PI Lewis, Sepp Hochreiter, Andreas Bender, Krishna C Bulusu, and Günter Klambauer. Deepsynergy: predicting anti-cancer drug synergy with deep learning. Bioinformatics, 34(9):1538–1546, 2018.

Guocai Chen, Alex Tsoi, Hua Xu, and W Jim Zheng. Predict effective drug combination by deep belief network and ontology fingerprints. Journal of Biomedical Informatics, 85:149–154, 2018.

Fangfang Xia, Maulik Shukla, Thomas Brettin, Cristina Garcia-Cardona, Judith Cohn, Jonathan E Allen, Sergei Maslov, Susan L Holbeck, James H Doroshow, Yvonne A Evrard, et al. Predicting tumor cell line response to drug pairs with deep learning. BMC Bioinformatics, 19(18):71–79, 2018.

Yejin Kim, Shuyu Zheng, Jing Tang, Wenjin Jim Zheng, Zhao Li, and Xiaoqian Jiang. Anticancer drug synergy prediction in understudied tissues using transfer learning. Journal of the American Medical Informatics Association, 28(1):42–51, 2021.

Theme 2: Improving Efficacy and Delivery of Gene Therapy

Task 1: CRISPR on-target outcome prediction

Task Description With a fixed target, given the gRNA sequence and other auxiliary information such as target gene expression and epigenetic profile, predict its on-target repair outcome.

Le Cong, F Ann Ran, David Cox, Shuailiang Lin, Robert Barretto, Naomi Habib, Patrick D Hsu, Xuebing Wu, Wenyan Jiang, Luciano A Marraffini, et al. Multiplex genome engineering using crispr/cas systems. Science, 339(6121):819–823, 2013.

Kristopher Torp Jensen, Lasse Fløe, Trine Skov Petersen, Jinrong Huang, Fengping Xu, Lars Bolund, Yonglun Luo, and Lin Lin. Chromatin accessibility and guide sequence secondary structure affect crispr-cas9 gene editing efficiency. FEBS Letters, 591(13):1892–1901, 2017.

Maurice Labuhn, Felix F Adams, Michelle Ng, Sabine Knoess, Axel Schambach, Emmanuelle M Charpentier, Adrian Schwarzer, Juan L Mateo, Jan-Henning Klusmann, and Dirk Heckl. Refined sgrna efficacy prediction improves large-and small-scale crispr–cas9 applications. Nucleic Acids Research, 46(3):1375–1385, 2018.

Miguel A Moreno-Mateos, Charles E Vejnar, Jean-Denis Beaudoin, Juan P Fernandez, Emily K Mis, Mustafa K Khokha, and Antonio J Giraldez. Crisprscan: designing highly efficient sgrnas for crispr-cas9 targeting in vivo. Nature Methods, 12(10):982–988, 2015.

Raj Chari, Prashant Mali, Mark Moosburner, and George M Church. Unraveling crispr-cas9 genome engineering parameters via a library-on-library approach. Nature Methods, 12(9):823–826, 2015.

Laurence OW Wilson, Daniel Reti, Aidan R O’Brien, Robert A Dunne, and Denis C Bauer. High activity target-site identification using phenotypic independent crispr-cas9 core functionality. The CRISPR Journal, 1(2):182–190, 2018.

Guohui Chuai, Hanhui Ma, Jifang Yan, Ming Chen, Nanfang Hong, Dongyu Xue, Chi Zhou, Chenyu Zhu, Ke Chen, Bin Duan, et al. Deepcrispr: optimized crispr guide rna design by deep learning. Genome Biology, 19(1):1–18, 2018.

Hui Kwon Kim, Seonwoo Min, Myungjae Song, Soobin Jung, Jae Woo Choi, Younggwang Kim, Sangeun Lee, Sungroh Yoon, and Hyongbum Henry Kim. Deep learning improves prediction of crispr–cpf1 guide rna activity. Nature Biotechnology, 36(3):239, 2018

Task 2: CRISPR off-target prediction

Task Description Given the gRNA sequence and the off-target DNA sequence, predict its off-target effect.

Xiao-Hui Zhang, Louis Y Tee, Xiao-Gang Wang, Qun-Shan Huang, and Shi-Hua Yang. Off-target effects in crispr/cas9-mediated genome engineering. Molecular Therapy-Nucleic Acids, 4:e264, 2015.

Florian Heigwer, Grainne Kerr, and Michael Boutros. E-crisp: fast crispr target site identification. Nature Methods, 11(2):122–123, 2014.

Sangsu Bae, Jeongbin Park, and Jin-Soo Kim. Cas-offinder: a fast and versatile algorithm that searches for potential off-target sites of cas9 rna-guided endonucleases. Bioinformatics, 30(10):1473–1475, 2014.

Patrick D Hsu, David A Scott, Joshua A Weinstein, F Ann Ran, Silvana Konermann, Vineeta Agarwala, Yinqing Li, Eli J Fine, Xuebing Wu, Ophir Shalem, et al. Dna targeting specificity of rna-guided cas9 nucleases. Nature Biotechnology, 31(9):827–832, 2013.

Maximilian Haeussler, Kai Schönig, Hélène Eckert, Alexis Eschstruth, Joffrey Mianné, Jean-Baptiste Renaud, Sylvie Schneider-Maunoury, Alena Shkumatava, Lydia Teboul, Jim Kent, et al. Evaluation of off-target and on-target scoring algorithms and integration into the guide rna selection tool crispor. Genome Biology, 17(1):1–12, 2016.

Thomas J Cradick, Peng Qiu, Ciaran M Lee, Eli J Fine, and Gang Bao. Cosmid: a web-based tool for identifying and validating crispr/cas off-target sites. Molecular Therapy-Nucleic Acids, 3:e214, 2014.

Jennifer Listgarten, Michael Weinstein, Benjamin P Kleinstiver, Alexander A Sousa, J Keith Joung, Jake Crawford, Kevin Gao, Luong Hoang, Melih Elibol, John G Doench, et al. Prediction of off-target activities for the end-to-end design of crispr guide rnas. Nature Biomedical Engineering, 2(1):38–47, 2018.

Jiecong Lin and Ka-Chun Wong. Off-target predictions in crispr-cas9 gene editing using deep learning. Bioinformatics, 34(17):i656–i663, 2018.

Task 3: Virus vector design

Task Description Given a set of virus sequences and their labels for a property X, obtain an accurate predictor oracle and conduct various generation modeling to generate de novo virus variants with a high score in X and high diversity.

Shyam Daya and Kenneth I Berns. Gene therapy using adeno-associated virus vectors. Clinical Microbiology Reviews, 21(4):583–593, 2008.

N Chirmule, KJ Propert, SA Magosin, Y Qian, R Qian, and JM Wilson. Immune responses to adenovirus and adeno-associated virus in humans. Gene Therapy, 6(9):1574–1583, 1999.

Eric D Kelsic and George M Church. Challenges and opportunities of machine-guided capsid engineering for gene therapy. Cell Gene Therapy Insights, 5:523–536, 2019.

Machine Learning for Genomics in Clinical Study

Theme 1: Translating Preclinical Animal Models to Humans

Task 1: Cross-species genotype-phenotype translation

Task Description : Given genotype-phenotype data of animals and only the genotype data of humans, train the model to fit phenotype from the genotype and transfer this model to human.

Sahin Naqvi, Alexander K Godfrey, Jennifer F Hughes, Mary L Goodheart, Richard N Mitchell, and David C Page. Conservation, acquisition, and functional impact of sex-biased gene expression in mammals. Science, 365(6450), 2019.

Kahn Rhrissorrakrai, Vincenzo Belcastro, Erhan Bilal, Raquel Norel, Carine Poussin, Carole Mathis, Rémi HJ Dulize, Nikolai V Ivanov, Leonidas Alexopoulos, J Jeremy Rice, et al. Understanding the limits of animal models as predictors of human biology: lessons learned from the sbv improver species translation challenge. Bioinformatics, 31(4):471–483, 2015.

Douglas K Brubaker, Elizabeth A Proctor, Kevin M Haigis, and Douglas A Lauffenburger. Computational translation of genomic responses from experimental model systems to humans. PLoS Computational Biology, 15(1):e1006286, 2019.

Rachelly Normand, Wenfei Du, Mayan Briller, Renaud Gaujoux, Elina Starosvetsky, Amit Ziv-Kenet, Gali Shalev-Malul, Robert J Tibshirani, and Shai S Shen-Orr. Found in translation: a machine learning model for mouse-to-human inference. Nature Methods, 15(12):1067–1073, 2018.

Victoria Yao, Rachel Kaletsky, William Keyes, Danielle E Mor, Aaron K Wong, Salman Sohrabi, Coleen T Murphy, and Olga G Troyanskaya. An integrative tissue-network approach to identify and test human disease genes. Nature Biotechnology, 36(11):1091–1099, 2018.

Edik M Blais, Kristopher D Rawls, Bonnie V Dougherty, Zhuo I Li, Glynis L Kolling, Ping Ye, Anders Wallqvist, and Jason A Papin. Reconciled rat and human metabolic networks for comparative toxicogenomics and biomarker predictions. Nature Communications, 8(1):1–15, 2017.

Theme 2: Curating High-quality Cohort

Task 1: Patient stratification/disease sub-typing

Task Description Given the gene expression and other auxiliary information for a set of patients produce criteria for patient stratification.

Ronglai Shen, Sijian Wang, and Qianxing Mo. Sparse integrative clustering of multiple omics data sets. The Annals of Applied Statistics, 7(1):269, 2013.

Daniela M Witten and Robert Tibshirani. A framework for feature selection in clustering. Journal of the American Statistical Association, 105(490):713–726, 2010.

Matan Hofree, John P Shen, Hannah Carter, Andrew Gross, and Trey Ideker. Network-based stratification of tumor mutations. Nature Methods, 10(11):1108–1115, 2013.

Yuan Gao and George Church. Improving molecular cancer class discovery through sparse non-negative matrix factorization. Bioinformatics, 21(21):3970–3975, 2005.

Runpu Chen, Le Yang, Steve Goodison, and Yijun Sun. Deep-learning approach to identifying cancer subtypes using high-dimensional genomic data. Bioinformatics, 36(5):1476–1483, 2020

Bo Wang, Aziz M Mezlini, Feyyaz Demir, Marc Fiume, Zhuowen Tu, Michael Brudno, Benjamin Haibe-Kains, and Anna Goldenberg. Similarity network fusion for aggregating data types on a genomic scale. Nature Methods, 11(3):333, 2014.

Philipp Jurmeister, Michael Bockmayr, Philipp Seegerer, Teresa Bockmayr, Denise Treue, Grégoire Montavon, Claudia Vollbrecht, Alexander Arnold, Daniel Teichmann, Keno Bressem, et al. Machine learning analysis of dna methylation profiles distinguishes primary lung squamous cell carcinomas from head and neck metastases. Science Translational Medicine, 11(509), 2019.

Li Li, Wei-Yi Cheng, Benjamin S Glicksberg, Omri Gottesman, Ronald Tamler, Rong Chen, Erwin P Bottinger, and Joel T Dudley. Identification of type 2 diabetes subgroups through topological analysis of patient similarity. Science Translational Medicine, 7(311):311ra174–311ra174, 2015.

Gilmer Valdes, José Marcio Luna, Eric Eaton, Charles B Simone, Lyle H Ungar, and Timothy D Solberg. Mediboost: a patient stratification tool for interpretable decision making in the era of precision medicine. Scientific Reports, 6(1):1–8, 2016.

Task 2: Matching patients for genome-driven trials

Task Description Given a pair of patient data (genomics, EHR, etc.) and trial eligibility criteria (text description), predict the matching likelihood.

John Mendelsohn, Harold L Moses, Sharyl J Nass, et al. A national cancer clinical trials system for the 21st century: reinvigorating the nci cooperative group program. 2010.

Vivek H Murthy, Harlan M Krumholz, and Cary P Gross. Participation in cancer clinical trials: race-, sex-, and age-based disparities. Jama, 291(22):2720–2726, 2004.

Simon J Craddock Lee, Caitlin C Murphy, Ann M Geiger, David E Gerber, John V Cox, Rasmi Nair, and Celette Sugg Skinner. Conceptual model for accrual to cancer clinical trials. Journal of Clinical Oncology, 37(23):1993, 2019.

Jessica J Tao, Michael H Eubank, Alison M Schram, Nicholas Cangemi, Erika Pamer, Ezra Y Rosen, Nikolaus Schultz, Debyani Chakravarty, John Philip, Jaclyn F Hechtman, et al. Real-world outcomes of an automated physician support system for genome-driven oncology. JCO Precision Oncology, 3:1–13, 2019.

Aurelia Bustos and Antonio Pertusa. Learning eligibility in cancer clinical trials using deep neural networks. Applied Sciences, 8(7):1206, 2018.

Junyi Gao, Cao Xiao, Lucas M Glass, and Jimeng Sun. Compose: Cross-modal pseudo-siamese network for patient trial matching. In KDD, pages 803–812, 2020.

Theme 3: Inferring Causal Effects

Task 1: Mendelian randomization

Task Description Given observation data of the genomic factor, exposure, outcome, and other auxiliary information formulate or identify the causal relations among them and compute the effect of the exposure to the outcome.

George Davey Smith and Shah Ebrahim. ‘mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease? International Journal of Epidemiology, 32(1):1–22, 2003.

Connor A Emdin, Amit V Khera, and Sekar Kathiresan. Mendelian randomization. Jama, 318(19):1925–1926, 2017.

Brian A Ference, Wonsuk Yoo, Issa Alesh, Nitin Mahajan, Karolina K Mirowska, Abhishek Mewada, Joel Kahn, Luis Afonso, Kim Allan Williams, and John M Flack. Effect of long-term exposure to lower low-density lipoprotein cholesterol beginning early in life on the risk of coronary heart disease: a mendelian randomization analysis. Journal of the American College of Cardiology, 60(25):2631–2639, 2012.

Marie Verbanck, Chia-yen Chen, Benjamin Neale, and Ron Do. Detection of widespread horizontal pleiotropy in causal relationships inferred from mendelian randomization between complex traits and diseases. Nature Genetics, 50(5):693–698, 2018.

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