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Freeware solutions to mixture interpretation and familial analysis. Thore Egeland Institute of forensic medicine University of Oslo EAFS Workshop, Sept 8, 2009, Glasgow. Background: LR (Paternity index). Essen-Möllers W: Posterior probabilities. Part 1: Unlinked markers: Familias.
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Freeware solutions to mixture interpretation and familial analysis Thore Egeland Institute of forensic medicine University of Oslo EAFS Workshop, Sept 8, 2009, Glasgow
Background: LR (Paternity index). Essen-Möllers W: Posterior probabilities. Part 1: Unlinked markers: Familias. Part 2: Linked markers: FEST. Part 3: Mixtures of relatives: R library forensic. Contents
LR (Paternity index ) H1: John Doe father. H2: Unknown man father. A,A B,B John Doe A,B
Essen-Möller’s W (posterior probability) H1: John Doe father. H2: Unknown man father. A,A B,B John Doe Flat prior A,B pB= 0,05
Several unlinked markers • Extends easily since multiplication is allowed.
Part 1: familias • Prior models. • Several potentially complex pedigrees. • Mutation model. • Theta-correction. • Silent alleles.
1 2 3 5 4 Complex pedigrees . Many hypotheses - 941, 942, 943 and 944 found dead. - Only 943 old enough to be a mother. - DNA-profiles available for 1,2,3,4 and 5. XX 943 XY 941 944 942
Modelling mutations • Mutation rate varies with • Sex of parent and locus.Alleles tend to mutate to close alleles:
Theta - correction General formula available.
Female A Child B Silent alleles. Classical example H1: Female mother H2: unrelated Silent allele S, i.e, Female A,S and Child B,S?
Egeland, T; Mostad, P; Mevåg, B; Stenersen, M: For Sci Int Vol 110, Nr. 1, 2000.
General DNA data Case related DNA Known relations Persons Pedigrees (calculations)
Unlinked markers may be insufficient • There are symmetric relations which cannot be resolved using unlinked autosomal markers. • There are distant family relationships that cannot be resolved since there are too few unlinked markers. • Haplotype data (Y, mtDNA) may sometimes help.
B B A A half-sibs grand parent-grand child • Problem (Thompson, 1986): • A and B share no, one or two alleles IBD with probabilities:0.5, 0.5, 0. • Identical likelihoods. B A uncle-niece 18
H1: A and B share a great-grandfather (HS-3-3 relation). H2: A and B unrelated. Distant family relationships
Linked markers needed L2 L1 r: recombination fraction,0: completely linked, 0.5: unlinked. cM 0 r Classical linkage analysis: L1: disease mutation, L2: genetic marker. Objective: determine L1-location We, however, only need null-likelihood 20
Part 3: Related contributors to mixtures • Family relationships must be accounted for when a typed contributor is related to an untyped contributor.
Symmetric cases. Untyped suspect • Assume a stain is available. There is typed victim V.The untyped suspect is a close relative of V: • H1:V+ half-sib • H2:V+uncle • H3:V+grand-father • These hypotheses can not be distinguished based on unlinked autosomal markers
Symmetric cases. Typed suspect • Assume next that the suspect S (half-sib) is typed and matches and that we consider • Hp:V+S, • Hd:V+unknown. • Normally evidence against S will be overwhelming. • Standard calculations, standard softwarelike DNAMIX can be used. • What happens if defence claims the perpetrator is a close relative?
Implemented by Miriam Marusiakova based on Hu and Fung (2003)
References • Buckleton, Triggs and Walsh (2005). CRC press. • Egeland, Mostad, Mevåg og Stenersen (2000).For Sci Int 110(1), 2000 • Familias: http://www.math.chalmers.se/~mostad/familias/ • Skare, Sheehan and Egeland. Bioinformatics (2009) • FEST: http://folk.uio.no/thoree/ • Hu and Fung (2003). Int J Leg Med 117(4) • R: forensic: http://cran.r-project.org/ (Author: Miriam Marusiakova)