A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations

Slides:



Advertisements
Similar presentations
Sofia A. Oliveira, Yi-Ju Li, Maher A
Advertisements

Recent Admixture in an Indian Population of African Ancestry
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single- Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite.
The Structure of Common Genetic Variation in United States Populations
Itsik Pe’er, Yves R. Chretien, Paul I. W. de Bakker, Jeffrey C
Genomic Patterns of Homozygosity in Worldwide Human Populations
Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q  Alex Desautels, Gustavo Turecki, Jacques Montplaisir, Adolfo.
Genetic Landscape of Eurasia and “Admixture” in Uyghurs
Michael W. Smith, Nick Patterson, James A. Lautenberger, Ann L
Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool  Luca Pagani, Toomas Kivisild, Ayele Tarekegn,
Chao Tian, David A. Hinds, Russell Shigeta, Sharon G
Population Genetic Structure of the People of Qatar
Soraya Beiraghi, Swapan K. Nath, Matthew Gaines, Desh D
Frances Busfield, David L. Duffy, Janine B. Kesting, Shelley M
Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p  Shenghan Chen, William G. Ondo, Shaoqi Rao,
CHEK2*1100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies 
High-Resolution Genetic Maps Identify Multiple Type 2 Diabetes Loci at Regulatory Hotspots in African Americans and Europeans  Winston Lau, Toby Andrew,
Comparing Algorithms for Genotype Imputation
Haplotype Estimation Using Sequencing Reads
Linkage Thresholds for Two-stage Genome Scans
A Combined Linkage-Physical Map of the Human Genome
Estimating Kinship in Admixed Populations
Caroline Durrant, Krina T. Zondervan, Lon R
So Many Correlated Tests, So Little Time
Association Mapping in Structured Populations
David H. Spencer, Kerry L. Bubb, Maynard V. Olson 
Accuracy of Haplotype Frequency Estimation for Biallelic Loci, via the Expectation- Maximization Algorithm for Unphased Diploid Genotype Data  Daniele.
Analysis of admixture in Native American populations from Colombia
Proportioning Whole-Genome Single-Nucleotide–Polymorphism Diversity for the Identification of Geographic Population Structure and Genetic Ancestry  Oscar.
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single- Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite.
Brian K. Maples, Simon Gravel, Eimear E. Kenny, Carlos D. Bustamante 
The American Journal of Human Genetics 
Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data  Gao T. Wang, Bo Peng, Suzanne M. Leal  The.
Ida Moltke, Matteo Fumagalli, Thorfinn S. Korneliussen, Jacob E
Volume 173, Issue 1, Pages e9 (March 2018)
Matching Strategies for Genetic Association Studies in Structured Populations  David A. Hinds, Renee P. Stokowski, Nila Patil, Karel Konvicka, David Kershenobich,
Robust Inference of Identity by Descent from Exome-Sequencing Data
Ellen E. Quillen, Mark D. Shriver  Journal of Investigative Dermatology 
Sriram Sankararaman, Swapan Mallick, Nick Patterson, David Reich 
Simultaneous Genotype Calling and Haplotype Phasing Improves Genotype Accuracy and Reduces False-Positive Associations for Genome-wide Association Studies 
Brian P. McEvoy, Joanne M. Lind, Eric T. Wang, Robert K
A Genetic Landscape Reshaped by Recent Events: Y-Chromosomal Insights into Central Asia  Tatiana Zerjal, R. Spencer Wells, Nadira Yuldasheva, Ruslan Ruzibakiev,
Genotype Imputation with Millions of Reference Samples
A Three–Single-Nucleotide Polymorphism Haplotype in Intron 1 of OCA2 Explains Most Human Eye-Color Variation  David L. Duffy, Grant W. Montgomery, Wei.
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design  Veronique Vitart,
Koji Suzuki, Tania Bustos, Richard A. Spritz 
Shuhua Xu, Wei Huang, Ji Qian, Li Jin 
Brian P. McEvoy, Joanne M. Lind, Eric T. Wang, Robert K
A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals  Brian L. Browning, Sharon.
A Fast, Powerful Method for Detecting Identity by Descent
Nonpaternity in Linkage Studies of Extremely Discordant Sib Pairs
A Genomewide Search Using an Original Pairwise Sampling Approach for Large Genealogies Identifies a New Locus for Total and Low-Density Lipoprotein Cholesterol.
Population Structure in Admixed Populations: Effect of Admixture Dynamics on the Pattern of Linkage Disequilibrium  C.L. Pfaff, E.J. Parra, C. Bonilla,
Benjamin A. Rybicki, José L. Walewski, Mary J
Human Population Genetic Structure and Inference of Group Membership
Jared R. Kohler, David J. Cutler 
Clive J. Hoggart, Esteban J. Parra, Mark D
L-GATOR: Genetic Association Testing for a Longitudinally Measured Quantitative Trait in Samples with Related Individuals  Xiaowei Wu, Mary Sara McPeek 
Trevor J. Pemberton, Chaolong Wang, Jun Z. Li, Noah A. Rosenberg 
Sriram Sankararaman, Swapan Mallick, Nick Patterson, David Reich 
Leslie S. Emery, Kevin M. Magnaye, Abigail W. Bigham, Joshua M
Yu Zhang, Tianhua Niu, Jun S. Liu 
Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations  Michael W. Smith, James A. Lautenberger, Hyoung.
Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies 
Recent Admixture in an Indian Population of African Ancestry
Enhanced Localization of Genetic Samples through Linkage-Disequilibrium Correction  Yael Baran, Inés Quintela, Ángel Carracedo, Bogdan Pasaniuc, Eran Halperin 
Genotype-Imputation Accuracy across Worldwide Human Populations
Mitochondrial DNA and Y Chromosome Variation Provides Evidence for a Recent Common Ancestry between Native Americans and Indigenous Altaians  Matthew C.
Population Genetic Structure of the People of Qatar
Mapping of a New SGBS Locus to Chromosome Xp22 in a Family with a Severe Form of Simpson-Golabi-Behmel Syndrome  L.M. Brzustowicz, S. Farrell, M.B. Khan,
Presentation transcript:

A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations Xianyun Mao, Abigail W. Bigham, Rui Mei, Gerardo Gutierrez, Ken M. Weiss, Tom D. Brutsaert, Fabiola Leon-Velarde, Lorna G. Moore, Enrique Vargas, Paul M. McKeigue, Mark D. Shriver, Esteban J. Parra  The American Journal of Human Genetics  Volume 80, Issue 6, Pages 1171-1178 (June 2007) DOI: 10.1086/518564 Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 1 Outline of the screening procedure for identification of AIMs The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 2 Scatterplots showing, for each chromosome, the physical location of the AIMs selected for the genomewide AM panel (X-axis) and the f values indicating the ancestry-information content for each marker (blackened squares). Scale is indicated on the right Y-axis. We also indicate the SNP density of the Affymetrix 500K mapping array (unblackened circles). Scale is indicated on the left Y-axis. The plotted f values are the averages of the f values between Europeans and Mesoamericans and the f values between Europeans and South Americans. The SNP density is measured using a sliding-window method with a 1-Mb window size and 200-kb offset. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 3 A, 3D PCO plot of the seven population samples included in this analysis (Europeans, Nahua from Mexico, Maya from Mexico, Quechua from Peru, Aymara/Quechua from Bolivia, West Africans, and East Asians), based on the allele-sharing distances between individuals estimated using 490,032 autosomal SNPs genotyped with the Affymetrix 500K Mapping Array. B, 3D PCO plot of the European and Native American populations, based on the allele-sharing distances between individuals estimated using 490,032 autosomal SNPs genotyped with the Affymetrix 500K Mapping Array. C, 3D PCO plot of the European and Native American populations, based on the allele-sharing distances between individuals estimated using the 2,120 AIMs selected for the Hispanic/Latino map. The proportion of variance explained by the first axis is indicated in each plot. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 4 Plot showing results of the analysis of the European and Native American samples with use of the program STRUCTURE, based on the genotype data for the 2,120 AIMs selected for the genomewide AM panel. The program was run using the linkage model, with 10,000 iterations for the burn-in phase and 50,000 iterations to collect parameter data. The model with two parental populations is the model that best fits the data. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions

Figure 5 Plot showing the relationship of f values and FIC values for the full panel of markers of the 500K array (A.1 and A.2) and the subset of markers with f values >0.3 (B.1 and B.2). Panels A.1 and B.1 show f values and FIC values with the assumption of a model with 75%:25% Mesoamerican:European ancestry, and panels A.2 and B.2 represent f values and FIC values with the assumption of a model with 25%:75% Mesoamerican:European ancestry. Spearman’s rank correlation coefficients (ρ) are indicated in bold above each panel. eu=European; ms=Mesoamerican. The American Journal of Human Genetics 2007 80, 1171-1178DOI: (10.1086/518564) Copyright © 2007 The American Society of Human Genetics Terms and Conditions