'Variant calling' diaporamas de présentation

Read mapping and variant calling in human short-read DNA sequences

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Canadian Bioinformatics Workshops

Canadian Bioinformatics Workshops. www.bioinformatics.ca. Module #: Title of Module. 2. Module 5 Big Data Analysis: Docker and PCAWG. Christina Yung, PhD Bioinformatics on Big Data: Computing on the Human Genome September 29 - 30, 2016. An image to represent your workshop or module.

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Omixon Workshops

Omixon Workshops. Considerations for Analyzing Targeted NGS Data - Introduction. Tim Hague, CEO. Targeted Data. Introduction. Many mapping, alignment and variant calling algorithms

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Considerations for Analyzing Targeted NGS Data Introduction

Considerations for Analyzing Targeted NGS Data Introduction. Tim Hague , CTO. Introduction. Many mapping, alignment and variant calling algorithms Most of these have been developed for whole genome sequencing and to some extent population genetic studi es. Premise.

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Genome and Exome Data Processing Tools

Tools used for genome and exome data processing.

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Exome and Genome Data Processing Tools

Exome and Genome Data Processing Tools

370 views • 26 slides

Why sequence tumors from mice?

Exome sequencing analysis of the mutational spectrum in carcinogen and genetic models of Kras -driven lung cancer. Peter Westcott, Kyle Halliwill, Minh To, David Quigley, Reyno Delrosario, Erik Fredlund, David Adams 1 , and Allan Balmain

376 views • 21 slides

Why sequence tumors from mice?

Exome sequencing analysis of the mutational spectrum in carcinogen and genetic models of Kras -driven lung cancer. Peter Westcott, Kyle Halliwill, Minh To, David Quigley, Reyno Delrosario, Erik Fredlund, David Adams 1 , and Allan Balmain

215 views • 21 slides

173 views • 8 slides