In the first part, we will address current computational methods for processing and analysing DNA sequencing data. In particular, we will focus on methods for the detection of genomic variation, i.e. differences between individual genome sequences. These differences include single nucleotide polymorphisms (SNPs), insertions/deletions, copy number variants, and genome rearrangements.
The second part will explore methods for quantitative proteome analysis using mass spectrometry, especially state-of-the-art multiplexing techniques (parallel processing of multiple analytes) vs. label-free methods, also considering experimental design and biomarker discovery. We will provide a number of relevant scientific articles and students will be expected to choose at least one for presentation in the seminar.
Where required we will have introduction talks to new technologies, before more involved topics are discussed.
|Instructor||Knut Reinert, Chris Bielow, Anne-Katrin Emde|
|Room||Arnimallee 6 SR 009|
|Start||Oct 18, 2011 | 02:00 PM|
Dienstag 14 - 16 Uhr
Vorbesprechung am 18.10. !