We propose to design and test mathematically well founded algorithmic and statistical tectonics for analyzing large scale, heterogeneous and noisy data. We focus on fully analytical evaluation of algorithms' performance and rigorous statistical guarantees on the analysis results. This project will leverage on the PIs' recent work on cancer genomics data analysis and rigorous data mining techniques. Those works were driven by specific applications, while in the current project we aim at developing general principles and techniques that will apply to a broad sets of applications. The proposed research is transformative in its emphasis on rigorous analytical evaluation of algorithms' performance and statistical measures of output uncertainty, in contrast to the primarily heuristic approaches currently used in data ming and machine learning. While we cannot expect full mathematical analysis of all data mining and machine learning techniques, any progress in that direction will have significant contribution to the reliability and scientific impact of this discipline. While ou work is motivated by molecular biology data, we expect the techniques to be useful for other scientific communities with massive multi-variate data analysis challenges. Molecular biology provides an excellent source of data for testing advance data analysis techniques: specifically, DNA/RNA sequence data repositories are growing at a super-exponential rate. The data is typically large and noisy, and it includes both genotype and phenotype features that permit experimental validation of the analysis. One such data repository is The Cancer Genome Atlas (TCGA), which we will use for initial testing of the proposed approaches.
This project will advocate a responsible approach to data analysis, based on well-founded mathematical and Statistical concepts. Such an approach enhances the effectiveness of evidence based medicine and other policy and social applications of big data analysis. The proposed work will be tested on human and cancer genome data, contributing to health IT, one of the National Priority Domain Areas.
| El-Kebir, Mohammed; Satas, Gryte; Raphael, Benjamin J (2018) Inferring parsimonious migration histories for metastatic cancers. Nat Genet 50:718-726 |
| Cancer Genome Atlas Research Network. Electronic address: andrew_aguirre@dfci.harvard.edu; Cancer Genome Atlas Research Network (2017) Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma. Cancer Cell 32:185-203.e13 |
| Nakka, Priyanka; Archer, Natalie P; Xu, Heng et al. (2017) Novel Gene and Network Associations Found for Acute Lymphoblastic Leukemia Using Case-Control and Family-Based Studies in Multiethnic Populations. Cancer Epidemiol Biomarkers Prev 26:1531-1539 |
| Leiserson, Mark D M; Reyna, Matthew A; Raphael, Benjamin J (2016) A weighted exact test for mutually exclusive mutations in cancer. Bioinformatics 32:i736-i745 |
| Vandin, Fabio; Raphael, Benjamin J; Upfal, Eli (2016) On the Sample Complexity of Cancer Pathways Identification. J Comput Biol 23:30-41 |
| El-Kebir, Mohammed; Satas, Gryte; Oesper, Layla et al. (2016) Inferring the Mutational History of a Tumor Using Multi-state Perfect Phylogeny Mixtures. Cell Syst 3:43-53 |
| Nakka, Priyanka; Raphael, Benjamin J; Ramachandran, Sohini (2016) Gene and Network Analysis of Common Variants Reveals Novel Associations in Multiple Complex Diseases. Genetics 204:783-798 |
| Leiserson, Mark D M; Wu, Hsin-Ta; Vandin, Fabio et al. (2015) CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer. Genome Biol 16:160 |
| Raphael, Benjamin J; Vandin, Fabio (2015) Simultaneous inference of cancer pathways and tumor progression from cross-sectional mutation data. J Comput Biol 22:510-27 |
| El-Kebir, Mohammed; Oesper, Layla; Acheson-Field, Hannah et al. (2015) Reconstruction of clonal trees and tumor composition from multi-sample sequencing data. Bioinformatics 31:i62-70 |
Showing the most recent 10 out of 14 publications
