Lincoln SE, Lander ES. Systematic detection of errors in genetic linkage data. Genomics. 1992;14(3):604-10.
Brown DM, Matise TC, Koike G, et al. An integrated genetic linkage map of the laboratory rat. Mamm Genome. 1998;9(7):521-30.
Mahtani MM, Widen E, Lehto M, et al. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nat Genet. 1996;14(1):90-4. doi:10.1038/ng0996-90
Dietrich WF, Radany EH, Smith JS, Bishop JM, Hanahan D, Lander ES. Genome-wide search for loss of heterozygosity in transgenic mouse tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16. Proc Natl Acad Sci U S A. 1994;91(20):9451-5.
Wapinski I, Pfeffer A, Friedman N, Regev A. Automatic genome-wide reconstruction of phylogenetic gene trees. Bioinformatics. 2007;23(13):i549-58. doi:10.1093/bioinformatics/btm193
Mikkelsen TS, Galagan JE, Mesirov JP. Improving genome annotations using phylogenetic profile anomaly detection. Bioinformatics. 2005;21(4):464-70. doi:10.1093/bioinformatics/bti027
Genovese G, Handsaker RE, Li H, Kenny EE, McCarroll SA. Mapping the human reference genome’s missing sequence by three-way admixture in Latino genomes. Am J Hum Genet. 2013;93(3):411-21. doi:10.1016/j.ajhg.2013.07.002
Weisenfeld NI, Yin S, Sharpe T, et al. Comprehensive variation discovery in single human genomes. Nat Genet. 2014;46(12):1350-5. doi:10.1038/ng.3121
Kamberov YG, Karlsson EK, Kamberova GL, et al. A genetic basis of variation in eccrine sweat gland and hair follicle density. Proc Natl Acad Sci U S A. 2015;112(32):9932-7. doi:10.1073/pnas.1511680112
Kruglyak L, Lander ES. High-resolution genetic mapping of complex traits. Am J Hum Genet. 1995;56(5):1212-23.