DNA Analysis Techniques for Molecular Genealogy. Luke Hutchison Project Supervisor: Scott R. Woodward

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Transcription:

DNA Analysis Techniques for Molecular Genealogy Luke Hutchison (lukeh@email.byu.edu) Project Supervisor: Scott R. Woodward

Mission: The BYU Center for Molecular Genealogy To establish the world s most comprehensive genetic and genealogical database. To create tools for reconstruction of genealogies from DNA To establish genetic links between families throughout the world.

Molecular Genealogy: Process 100,000 DNA samples and genealogies are being collected from 500 different populations Common ancestors and population structure are inferred [population and quantitative genetics] A searchable database is being produced for DNA-based genealogical research

?

Common Ancestor (Suffolk, England, ca. 1893: 33%; Glasgow, Scotland, ca. 1905: 12%;...) Unknown genealogy

What is the Basis of Molecular Genealogy? Each individual carries within their DNA a record of who they are and how they are related to all other people. You received all of your DNA from your two parents (50% from each). Specific regions of DNA have properties that can: Identify an individual Link them to a family Identify extended family groups (tribes or clans)

3 major types of genetic data Y Chromosome Males only, paternal inheritance Haploid, none or little recombination 0.51% of an individual's total genetic information Mitochondrial DNA Both males and females, maternal inheritance Haploid, none or little recombination 0.0006% of an individual's total genetic information Autosomal (Nuclear) Both males and females, inherited equally from both parents Diploid, undergoes recombination at each generation >99% of your genetic information

Y chromosome Autosomal (nuclear) Mitochondrial

Genotypic and Genealogical data 8562 276 280 261 273 162 166 111 125 205 205 207 213 134 134 170 174 222 224 265 269 266 274 118 122 141 149 134 138 175 179 187 195 8563 288 291 271 275 148 160 127 127 209 211 211 223 136 150 174 178 224 224 261 273 268 268 106 120 125 133 132 138 176 178 201 203 8564 272 291 259 267 144 156 113 127 209 211 207 211 142 154 152 174 218 224 269 273 272 272 100 122 149 149 140 140 174 179 191 201 8565 291 295 263 275 148 160 123 127 207 211 217 217 134 136 174 174 220 224 269 309 262 272 106 120 143 147 136 138 171 175 191 195 8566 271 271 263 271 162 164 111 113 207 209 209 213 150 150 174 178 212 216 273 277 258 262 102 118 127 145 138 140 173 175 191 195 8567 271 283 269 275 162 164 111 127 207 209 207 217 150 156 170 178 212 216 273 309 258 270 102 104 143 145 130 138 173 175 187 191 8549 1 8 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 Unknown 0.125 8550 1 8 Unknown 0.125 Unknown 0.125 Unknown 0.125 Unknown 0.125 Unknown 0.125 Unknown 0.125 Unknown 0.125 Unknown 0.125 8551 1 8 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 Europe 0.125 Europe 0.125 NorthAmerica 0.125 NorthAmerica 0.125 8552 1 8 Europe 0.125 Europe 0.125 Unknown 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 NorthAmerica 0.125 8553 1 8 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 8554 1 8 PacificIsland 0.125 PacificIsland 0.125 Unknown 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125 PacificIsland 0.125

Sequence and Length polymorphisms

Types of DNA Data Extracted Pair of alleles (numbers of repeats) for a locus (e.g.. 121,123) Linked loci (close together in chromosome) Unlinked loci (distant enough from each other to be genetically unrelated, due to the high probability of a crossover occurring between the markers; the presence of one does not imply the presence of the other)

Linked Loci: Haplotypes The probability of a crossover event occurring in the middle of a haplotype is low, since the loci are tightly linked. Haplotypes are therefore likely to be passed down intact for many generations.

Haplotyping Problem: Correct order of the genetic information in a pair is unknown (which allele came from which parental chromosome?): 121,123 123 or 123,121 121? The problem compounds for linked loci: 121 123 123 121 123 123 123 121 121 } 142 144 144 144 142 142 142 144 144 }... (x 2³=8) 115 119 119 115 119 119 115 119 119 } Finding which alleles occur together on the same chromosome for linked loci (the haplotypes) is called hapotyping.. The alignment is called the phase.

Properties of Haplotypes Populations which do not inter-breed each develop a distinctive distribution of haplotypes. Haplotypes may eventually appear (due to mutation and/or crossover) that do not exist in any other population Haplotypes give much more discerning power than alleles alone, since there are many possible haplotypes given a set of possible alleles at each locus

Haplotyping: A Cyclic Problem We could figure out the most likely phase for the alleles in a haplotype if we knew the haplotype distributions of the parent populations? We could figure out the haplotype distributions of the parent populations if we knew the correct phase of the alleles

Haplotyping: A Cyclic Solution (1) First guess for phase probs: all equal (0.125) (3), (5),... Estimate phase probabilities based on the current estimate of population haplotype probabilities (2), (4),... Estimate population haplotype probabilities based on the current estimate of phase probabilities

Haplotyping: Results Convergence typically achieved in 3-7 iterations Difficult to judge accuracy since nobody knows how to get the true correct answer! Previous researchers attempts on simulated data: 50-60% accuracy Our algorithm on (different) simulated data: 97% Our algorithm on real data (accuracy measured by 'spiking' with CEPH data): 88-93%

How to Contact Us E-mail: molecular-genealogy@email.byu.edu Phone: 801-378-1245 Mail: 788 WIDB BYU Provo, UT 84602 Web: http://molecular-genealogy.byu.edu