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Raw sequencer output alignment - PowerPoint PPT Presentation

Use of NGS to identify the causal variant associated with a complex phenotype

Use of NGS to identify the causal variant associated with a complex phenotype. Overview. Why are we sequencing? How did we select the animals to sequence? What are the steps involved in the process? What do you do with the reads once you have them? Where are we now?. Introduction.

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510 views • 40 slides

Tools to Exploit Sequence data to find new markers and Disease Loci in Cattle

Tools to Exploit Sequence data to find new markers and Disease Loci in Cattle. D. M. Bickhart , H. A. Lewin and G. E. Liu. Amount of sequence data. ~ 312500 Human genome equivalents. ~ 312.5 Human genome equivalents. SRA chart From Wikipedia Commons . Why sequence DNA?.

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282 views • 19 slides

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Raw sequencer output alignment - PowerPoint PPT Presentation

Use of NGS to identify the causal variant associated with a complex phenotype

Tools to Exploit Sequence data to find new markers and Disease Loci in Cattle