Inference platform for Ancestry Informative Markers

23 mins 17 secs,  42.61 MB,  MP3  44100 Hz,  249.87 kbits/sec
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Description: Torben Tvedebrink
Wednesday 9th November 2016 - 12:30 to 13:00
 
Created: 2016-11-11 16:01
Collection: Probability and Statistics in Forensic Science
Publisher: Isaac Newton Institute
Copyright: Torben Tvedebrink
Language: eng (English)
Distribution: World     (downloadable)
Explicit content: No
Aspect Ratio: 16:9
Screencast: No
Bumper: UCS Default
Trailer: UCS Default
 
Abstract: Co-authors: Poul Svante Eriksen (Aalborg University), Helle Smidt Mogensen (University of Copenhagen), Niels Morling (University of Copenhagen)

In this talk I will present a platform for making inference about Ancestry Informative Markers (AIMs), which are a panel of SNP markers used in forensic genetics to infer the population origin of a given DNA profile.

Several research groups have proposed such AIM panels, each with a specific objective in mind. Some were designed to discriminate between closely related ethnic groups whereas other focus on larger distances (more remotely located populations). This talk is not about selecting markers or populations for testing. The focus will be about how to provide forensic geneticists with a tool that can be used to infer the most likely population(s) of a given DNA profile.

By the use of R (www.r-project.org) and Shiny (web applications framework for R, RStudio) I have developed a platform that provides the numerical and visual output necessary for the geneticist to analyse and report the genetic evidence.

In the talk I will discuss the evidential weight in this situation and uncertainties in population frequencies. As the database of populations is not exhaustive, there is no guarantee that there exists a \textsl{relevant} population in the database, where \textsl{relevant} means a population sufficiently close to the \textsl{true} population. We derive a database score specific for each DNA profile and use this score to assess the relevance of the database relative to the DNA profile.
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