PADRE: Pedigree-Aware Distant-Relationship Estimation.

[1]  A. Price,et al.  Leveraging distant relatedness to quantify human mutation and gene conversion rates , 2015, bioRxiv.

[2]  Jeffrey Staples,et al.  PRIMUS: rapid reconstruction of pedigrees from genome-wide estimates of identity by descent. , 2014, American journal of human genetics.

[3]  Ellen M Wijsman,et al.  Combining Family‐ and Population‐Based Imputation Data for Association Analysis of Rare and Common Variants in Large Pedigrees , 2014, Genetic epidemiology.

[4]  H. Joe,et al.  Model comparison with composite likelihood information criteria , 2014, 1410.4354.

[5]  Gustavo Glusman,et al.  A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data , 2014, Nature Biotechnology.

[6]  Ross M. Fraser,et al.  A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness , 2014, PLoS genetics.

[7]  Shankaracharya,et al.  Relationship Estimation from Whole-Genome Sequence Data , 2014, PLoS genetics.

[8]  Mohamad Saad,et al.  Power of Family‐Based Association Designs to Detect Rare Variants in Large Pedigrees Using Imputed Genotypes , 2014, Genetic epidemiology.

[9]  J. Morrison Characterization and Correction of Error in Genome‐Wide IBD Estimation for Samples with Population Structure , 2013, Genetic epidemiology.

[10]  D. Nickerson,et al.  Utilizing Graph Theory to Select the Largest Set of Unrelated Individuals for Genetic Analysis , 2013, Genetic epidemiology.

[11]  Blair H. Smith,et al.  Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study , 2013, BMC Medical Genetics.

[12]  Brian L Browning,et al.  Identity by descent between distant relatives: detection and applications. , 2012, Annual review of genetics.

[13]  E. Wijsman The role of large pedigrees in an era of high-throughput sequencing , 2012, Human Genetics.

[14]  Jochen Musch,et al.  Estimating the Prevalence of Nonpaternity in Germany , 2012, Human nature.

[15]  M J Alvarez-Cubero,et al.  Genetic Identification of Missing Persons: DNA Analysis of Human Remains and Compromised Samples , 2012, Pathobiology.

[16]  Sharon R. Browning,et al.  Detecting Rare Variant Associations by Identity-by-Descent Mapping in Case-Control Studies , 2012, Genetics.

[17]  B. Browning,et al.  A fast, powerful method for detecting identity by descent. , 2011, American journal of human genetics.

[18]  Jinchuan Xing,et al.  Maximum-likelihood estimation of recent shared ancestry (ERSA). , 2011, Genome research.

[19]  D. Altshuler,et al.  A map of human genome variation from population-scale sequencing , 2010, Nature.

[20]  Sharon R Grossman,et al.  Integrating common and rare genetic variation in diverse human populations , 2010, Nature.

[21]  P. Shannon,et al.  Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing , 2010, Science.

[22]  Alexander Gusev,et al.  Whole population, genome-wide mapping of hidden relatedness. , 2009, Genome research.

[23]  B. Browning,et al.  Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. , 2007, American journal of human genetics.

[24]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[25]  Eric P. Xing,et al.  Interpreting anonymous DNA samples from mass disasters - probabilistic forensic inference using genetic markers , 2006, ISMB.

[26]  M. Bellis,et al.  Measuring paternal discrepancy and its public health consequences , 2005, Journal of Epidemiology and Community Health.

[27]  J. Pritchard,et al.  Confounding from Cryptic Relatedness in Case-Control Association Studies , 2005, PLoS genetics.

[28]  M. Boehnke,et al.  Accurate inference of relationships in sib-pair linkage studies. , 1997, American journal of human genetics.