Many projects in the genomics field rely on increasingly large data sets, analyzing, for example, genomes of thousands of individuals affected by a particular disease. It is paramount to understand how large data sets can be managed and processed in an efficient way and how next-generation sequencing processing pipelines and workflows can be used to benefit such large-scale projects. In this course, we will introduce some of the existing technologies, tools and platforms available for this aim, including Apache Spark, GMQL, Amazon WS, Galaxy, and KNIME. We will also discuss some examples of software libraries in different programming languages (mainly Python and R) that can help to design own tools and pipelines.
Risultati apprendimento attesi
Given the vastness of the topics presented, the ultimate goal of the course is not going in-depth in specific analysis approaches to genomic big data analysis, but rather providing a broad overview of different solutions paired with the understanding of strengths and weaknesses of different methodologies, to help developing the understanding of which solutions might be appropriate for a specific problem at hand.
Periodo: Primo semestre
(se vi sono più edizioni controllare anche il periodo dell'edizione, che può essere diverso)
- Main concepts and issues (4 hours): challenges that need to be addressed; advantages of workflow management for big data applications; multi-source and heterogeneous data integration; reproducibility of results.
- Querying and extracting heterogeneous big genomic data (6 + 6 hours): - Genomic Data Model (GDM) and GenoMetric Query Language (GMQL) - Main operational features of GMQL and GMQL repository - GMQL interfaces: GMQL Web, GMQL APIs, pyGMQL and RGMQL - Integrative analysis of heterogeneous (epi)genomics data with GMQL, Python and R/Bioconductor
- Workflow management systems for biomedical applications (6 + 6 hours): - Galaxy - KNIME - Brief overview of other systems
- Distributed programming with Apache Spark (6 + 4 hours): - Introduction to distributed processing on the cloud and motivation - Main features of Apache Spark - Spark APIs for Pyhton and R
- Pattern mining, search and analysis of heterogeneous big (epi)genomic data (6 + 4 hours): - Hidden Markow Models for state pattern analysis - Chromatin state discovery with: ChromHMM and Segway - Searching similar feature patterns in multiple genome browser tracks - Integrated Genome Browser (IGB) and the SimSearch plugin
- Data processing with cloud computing services (4 hours): - Introduction to cloud computing for genomics - Amazon Web Services (AWS) and similar services
- Use cases / example analyses of heterogeneous data (2 + 4 hours)
Knowledge of programming, preferable in Python language and/or in R. Knowledge in molecular biology.
Class lectures and exercises in an informatics room using the student's laptop. All used data and tools are publicly available.
Materiale di riferimento
The slides presented during the course and the estimated detailed schedule of lectures and practices are available on the "Be e-Poli" (BeeP), the portal for the network activities of students and professors at the Politecnico di Milano, accessible from the Politecnico di Milano Web site; students registered to the course for the current academic year can access it.
Recommended articles (not required to pass the exam): - Batut et al. (2018) Community-driven data analysis training for biology. Cell Systems 6: 752-758. - Fillbrunn et al. (2017) KNIME for reproducible cross-domain analysis of life science data. Journal of Biotechnology 261: 149-156. - Grüning et al. (2018) Practical bomputational reproducibility in the life sciences. Cell Systems 6(6): P631-P635. - Hoffman et al. (2012) Unsupervised pattern discovery in human chromatin structure through genomic segmentation. Nat Methods 9(5): 473-476. - Kulkarni and Frommolt (2017) Challenges in the setup of large-scale Next-Generation Sequencing analysis workflows. Computational and Structural Biotechnology Journal 15: 471-477. - Langmead et al. (2018) Cloud computing as a platform for genomic data analysis and collaboration. Nat Rev Genet 19(4): 208-219. - Li et al. (2015) An NGS workflow blueprint for DNA sequencing data and its application in individualized molecular oncology. Cancer Informatics 14(S5): 87-107.
Modalità di verifica dell’apprendimento e criteri di valutazione
The assessment is based on a written exam at the end of the course, with exercises and open questions on all the topics presented during the course.