Single nucleotide polymorphisms and recombination rate in humans.
暂无分享,去创建一个
[1] W Stephan,et al. The hitchhiking effect on the site frequency spectrum of DNA polymorphisms. , 1995, Genetics.
[2] W. Stephan,et al. Joint effects of genetic hitchhiking and background selection on neutral variation. , 2000, Genetics.
[3] W. Stephan,et al. Analysis of a genetic hitchhiking model, and its application to DNA polymorphism data from Drosophila melanogaster. , 1993, Molecular biology and evolution.
[4] N L Kaplan,et al. Deleterious background selection with recombination. , 1995, Genetics.
[5] D. Hewett‐Emmett,et al. High polymorphism at the human melanocortin 1 receptor locus. , 1999, Genetics.
[6] F. Tajima. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. , 1989, Genetics.
[7] M. Kimura,et al. The neutral theory of molecular evolution. , 1983, Scientific American.
[8] E. Boerwinkle,et al. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. , 1998, American journal of human genetics.
[9] D. Mccormick. Sequence the Human Genome , 1986, Bio/Technology.
[10] Timothy B. Stockwell,et al. The Sequence of the Human Genome , 2001, Science.
[11] J. Hey,et al. X chromosome evidence for ancient human histories. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[12] G. Gyapay,et al. A radiation hybrid map of the human genome. , 1996, Human molecular genetics.
[13] M. Nachman,et al. Contrasting evolutionary histories of two introns of the duchenne muscular dystrophy gene, Dmd, in humans. , 2000, Genetics.
[14] J. Armour,et al. A highly variable segment of human subterminal 16p reveals a history of population growth for modern humans outstide Africa. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[15] G. A. Watterson. On the number of segregating sites in genetical models without recombination. , 1975, Theoretical population biology.
[16] M. Nei,et al. Mathematical model for studying genetic variation in terms of restriction endonucleases. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[17] M. Rieder,et al. Sequence variation in the human angiotensin converting enzyme , 1999, Nature Genetics.
[18] Doron Lancet,et al. Dichotomy of single-nucleotide polymorphism haplotypes in olfactory receptor genes and pseudogenes , 2000, Nature Genetics.
[19] M. Nachman,et al. Microsatellite variation and recombination rate in the human genome. , 2000, Genetics.
[20] R. Griffiths,et al. Archaic African and Asian lineages in the genetic ancestry of modern humans. , 1997, American journal of human genetics.
[21] D. Cooper,et al. Human Gene Mutation , 1993 .
[22] B. Charlesworth,et al. The effect of deleterious mutations on neutral molecular variation. , 1993, Genetics.
[23] L. Jin,et al. Worldwide Dna Sequence Variation in a 10-kilobase Noncoding Region on Human Chromosome 22 Materials and Methods Dna Samples. Sixty-four Individuals Were Collected Worldwide from 16 Populations in Four Major Geographic Areas, including 20 , 2022 .
[24] P. Donnelly,et al. Optimal sequencing strategies for surveying molecular genetic diversity. , 1996, Genetics.
[25] K. Kidd,et al. Evolution of a HOXB6 intergenic region within the great apes and humans. , 1999, Journal of human evolution.
[26] T. Jukes,et al. The neutral theory of molecular evolution. , 2000, Genetics.
[27] N L Kaplan,et al. The "hitchhiking effect" revisited. , 1989, Genetics.
[28] M. Daly,et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.
[29] M. Nachman,et al. DNA variability and recombination rates at X-linked loci in humans. , 1998, Genetics.
[30] J. M. Smith,et al. The hitch-hiking effect of a favourable gene. , 1974, Genetical research.
[31] P. Deloukas,et al. Comparison of human genetic and sequence-based physical maps , 2001, Nature.
[32] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[33] R. Hudson,et al. Adjusting the focus on human variation. , 2000, Trends in genetics : TIG.
[34] T. Wiehe. The effect of selective sweeps on the variance of the allele distribution of a linked multiallele locus: hitchhiking of microsatellites. , 1998, Theoretical population biology.
[35] E. Boerwinkle,et al. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. , 2000, American journal of human genetics.
[36] A. Clark,et al. Local rates of recombination are positively correlated with GC content in the human genome. , 2001, Molecular biology and evolution.
[37] Henrik Kaessmann,et al. DNA sequence variation in a non-coding region of low recombination on the human X chromosome , 1999, Nature Genetics.
[38] D. Begun,et al. Reduced X-linked nucleotide polymorphism in Drosophila simulans. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[39] S. Tavaré,et al. Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy. , 1999, Genetics.
[40] B. Trask,et al. A High-Resolution Radiation Hybrid Map of the Human Genome Draft Sequence , 2001, Science.
[41] B. Charlesworth,et al. The pattern of neutral molecular variation under the background selection model. , 1995, Genetics.
[42] A. Di Rienzo,et al. Detection of the signature of natural selection in humans: evidence from the Duffy blood group locus. , 2000, American journal of human genetics.
[43] Wen-Hsiung Li,et al. Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1. , 2001, Molecular biology and evolution.
[44] C. Aquadro,et al. Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster , 1992, Nature.