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Proteomic Technologies, Crucial Roles, Expression of Genes, Pyrosequencing and Illumina, Sequencing Technology, Dimensional Difference Gel Electrophoresis, Isotope Coded Affinity Tagging, Multidimensional Protien Identification Tool, Isobaric Tags for Relative and Accurate Quantification. What description should I write more when I have done so much work already?
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“Epigenetic marks and RNA interference play crucial roles in modulating the expression of genes”. Explain this statement using appropriate examples, and describe how the various mechanisms are co-ordinated.
Compare and contrast pyrosequencing and Illumina based next generation sequencing technology (NGS). Give an example of the use of NGS in genomics.
Critically consider the advantages and disadvantages of three of the following proteomic technologies: Two dimensional Difference Gel Electrophoresis (2D-DiGE) Isotope Coded Affinity Tagging (ICAT) Multidimensional Protien Identification Tool (MudPIT) Isobaric Tags for Relative and Accurate Quantification (iTRAQ)
Focusing on one specific type of mass spectrometer instrument, explain in broad terms operation of the ion source and analyser. Outline the format of typical data generated by this instrument in metabolomics experiments.
Explain how the use of markers and comparative genomics lead to the isolation of the staygreen gene in Arabidopsis.
Examine the following figure showing a Boolean description of the regulation of some key genes involved in plant defence against pathogens by some key hormones (boxed). For each gene discuss how they are regulated based on your understanding of Boolean gates.
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Figure 1: The regulation of some plant defence genes described using Boolean gates.