Excap: maximization of haplotypic diversity of linked markers.

Genetic markers, defined as variable regions of DNA, can be utilized for distinguishing individuals or populations. As long as markers are independent, it is easy to combine the information they provide. For nonrecombinant sequences like mtDNA, choosing the right set of markers for forensic applicat...

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Main Authors: André Kahles, Fahad Sarqume, Peter Savolainen, Lars Arvestad
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3820696?pdf=render
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author André Kahles
Fahad Sarqume
Peter Savolainen
Lars Arvestad
author_facet André Kahles
Fahad Sarqume
Peter Savolainen
Lars Arvestad
author_sort André Kahles
collection DOAJ
description Genetic markers, defined as variable regions of DNA, can be utilized for distinguishing individuals or populations. As long as markers are independent, it is easy to combine the information they provide. For nonrecombinant sequences like mtDNA, choosing the right set of markers for forensic applications can be difficult and requires careful consideration. In particular, one wants to maximize the utility of the markers. Until now, this has mainly been done by hand. We propose an algorithm that finds the most informative subset of a set of markers. The algorithm uses a depth first search combined with a branch-and-bound approach. Since the worst case complexity is exponential, we also propose some data-reduction techniques and a heuristic. We implemented the algorithm and applied it to two forensic caseworks using mitochondrial DNA, which resulted in marker sets with significantly improved haplotypic diversity compared to previous suggestions. Additionally, we evaluated the quality of the estimation with an artificial dataset of mtDNA. The heuristic is shown to provide extensive speedup at little cost in accuracy.
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spelling doaj.art-42df63ee49d24ddca4cade1d4791ade02022-12-21T19:02:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e7901210.1371/journal.pone.0079012Excap: maximization of haplotypic diversity of linked markers.André KahlesFahad SarqumePeter SavolainenLars ArvestadGenetic markers, defined as variable regions of DNA, can be utilized for distinguishing individuals or populations. As long as markers are independent, it is easy to combine the information they provide. For nonrecombinant sequences like mtDNA, choosing the right set of markers for forensic applications can be difficult and requires careful consideration. In particular, one wants to maximize the utility of the markers. Until now, this has mainly been done by hand. We propose an algorithm that finds the most informative subset of a set of markers. The algorithm uses a depth first search combined with a branch-and-bound approach. Since the worst case complexity is exponential, we also propose some data-reduction techniques and a heuristic. We implemented the algorithm and applied it to two forensic caseworks using mitochondrial DNA, which resulted in marker sets with significantly improved haplotypic diversity compared to previous suggestions. Additionally, we evaluated the quality of the estimation with an artificial dataset of mtDNA. The heuristic is shown to provide extensive speedup at little cost in accuracy.http://europepmc.org/articles/PMC3820696?pdf=render
spellingShingle André Kahles
Fahad Sarqume
Peter Savolainen
Lars Arvestad
Excap: maximization of haplotypic diversity of linked markers.
PLoS ONE
title Excap: maximization of haplotypic diversity of linked markers.
title_full Excap: maximization of haplotypic diversity of linked markers.
title_fullStr Excap: maximization of haplotypic diversity of linked markers.
title_full_unstemmed Excap: maximization of haplotypic diversity of linked markers.
title_short Excap: maximization of haplotypic diversity of linked markers.
title_sort excap maximization of haplotypic diversity of linked markers
url http://europepmc.org/articles/PMC3820696?pdf=render
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