29901 Scientific Computing for Life Scientists and Metabolic Modeling for Cell Factory Design

2017/2018

Kursusinformation
Scientific Computing for Life Scientists and Metabolic Modeling for Cell Factory Design
Engelsk
2,5
Ph.d., Fagligt fokuseret kursus
Kurset udbydes under tompladsordningen
Uge 37 (10.9 – 14.9.2018)
Campus Lyngby
35 hours computer exercises, 14 hours reading prior and during the course, 35 hours individual project (application of learned skills to a target product and host organism or analysis of a data set to be picked by the student) and preparation of report.
[Kurset følger ikke DTUs normale skemastruktur]
Aftales med underviser
Bedømmelse af opgave(r)/rapport(er)
The students will apply the learned skills to projects of their own choosing. To pass they will have to hand in reports that demonstrate the successful application of the tools and methods covered in the course (4 weeks).
Alle hjælpemidler er tilladt :

Weekly follow-up meetings will be organized to assist the students.

bestået/ikke bestået , intern bedømmelse
27824
Minimum 5 Maksimum: 15
Nikolaus Sonnenschein , Lyngby Campus, Bygning 220 , niso@biosustain.dtu.dk
Kai Blin , Lyngby Campus, Bygning 220 , kblin@biosustain.dtu.dk
Nils Henning Redestig

29 DTU Biosustain
I studieplanlæggeren
Overordnede kursusmål
Provide the student with the computational skills needed to survie in data-rich cell factory engineering projects.
Læringsmål
En studerende, der fuldt ud har opfyldt kursets mål, vil kunne:
  • To use the Unix shell for working with files and directories, pipes and filters, loops, shell scripts, and searching.
  • Use Python and R for data analysis and task automation, including the import of libraries, reading and plotting of data, selection and filtering of data, writing of conditional statements and functions, and debugging.
  • Utilize basic version control of data and programming code with Git.
  • Import, manipulate, and simulate genome-scale metabolic models.
  • Calculate theoretical maximum yields for different products, host organisms, and feed
  • Predict gene knockout strategies.
  • Compute over-expression and down-regulation targets.
  • Enumerate heterologous pathways and assess their thermodynamic feasibility.
  • Integrate transcriptomics (and other types of omics) data into genome-scale metabolic models.
  • Simulate batch growth using dynamic flux balance analysis.
Kursusindhold
With data generation becoming evermore easy in biology, life scientists and engineers are increasingly facing challenges in analyzing data in their line of work. For example, simple bioinformatics tasks can become a huge drain on scientists’ time as they repetitively copy and paste information into web interfaces instead of running batch operations.
Furthermore, with genetic manipulations becoming evermore easy to carry out, qualifications demanded of cell factory engineers will shift away from the ability to construct strains towards analysis of data and design of new strains, a trend that is only going to be accelerated with DNA synthesis costs plummeting and lab automation becoming more widely available. Therefore, it will be essential that the next generation of PhD students in cell factory engineering are trained in computational tools needed for data analysis and strain design.

As a first step towards this goal, two courses (two days each) will be held back to back:
1. A Software Carpentry course that covers basic computational skills and specifically targets life scientists (task automatization, command line usage, programming with Python, data analysis with R, version control etc.). Since 1998, Software Carpentry has been teaching basic lab skills for research computing to scientists and engineers and course materials have continuously been adapted and tailored to their problems and needs.
2. Taking advantage of the materials covered in (1), a computational cell factory design course that covers basic genome-scale metabolic modeling and in silico strain design methods will be held for people involved in strain engineering projects or metabolic research in general.
Litteraturhenvisninger
http:/​/​software-carpentry.org/​lessons/​

Lewis, N. E., Nagarajan, H., & Palsson, B. Ø. (2012). Constraining the metabolic genotype-phenotype relationship using a phylogeny of in silico methods. Nature Reviews Microbiology, 10(4), 291–305. http:/​/​doi.org/​10.1038/​nrmicro2737

Bordbar, A., Monk, J. M., King, Z. A., & Palsson, B. Ø. (2014). Constraint-based models predict metabolic and associated cellular functions. Nature Reviews Genetics, 15(2), 107–120. http:/​/​doi.org/​10.1038/​nrg3643

Maia, P., Rocha, M., & Rocha, I. (2016). In Silico Constraint-Based Strain Optimization Methods: the Quest for Optimal Cell Factories. Microbiology and Molecular Biology Reviews : MMBR, 80(1), 45–67. http:/​/​doi.org/​10.1128/​MMBR.00014-15
Sidst opdateret
23. februar, 2018