Abstract
Recent technologies for typing single nucleotide polymorphisms (SNPs) across a population are producing genome-wide genotype data for tens of thousands of SNP sites. The emergence of such large data sets underscores the importance of algorithms for large-scale haplotyping. Common haplotyping approaches first partition the SNPs into blocks of high linkage-disequilibrium, and then infer haplotypes for each block separately. We investigate an integrated haplotyping approach where a partition of the SNPs into a minimum number of non-contiguous subsets is sought, such that each subset can be haplotyped under the perfect phylogeny model. We show that finding an optimum partition is
-hard even if we are guaranteed that two subsets suffice. On the positive side, we show that a variant of the problem, in which each subset is required to admit a perfect path phylogeny haplotyping, is solvable in polynomial time.
-hard even if we are guaranteed that two subsets suffice. On the positive side, we show that a variant of the problem, in which each subset is required to admit a perfect path phylogeny haplotyping, is solvable in polynomial time.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Discrete Mathematics |
| Jahrgang | 2009 |
| Ausgabenummer | 309(18) |
| Seiten (von - bis) | 5610-5617 |
| Publikationsstatus | Veröffentlicht - 2009 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 9 – Industrie, Innovation und Infrastruktur
Projekte
- 1 Abgeschlossen
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Komplexität von Haplotypisierungsproblemen
Tantau, T. (Projektleiter*in (PI)), Schnoor, I. (Beteiligte*r Wissenschaftler*in), Elberfeld, M. (Beteiligte*r Wissenschaftler*in), Kuczewski, J. (Beteiligte*r Wissenschaftler*in) & Pohlmann, J. (Beteiligte Person)
01.01.05 → 31.12.10
Projekt: DFG Einzelprojekte › DFG Einzelförderungen (Sachbeihilfen)
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