Chromosomal haplotypes by genetic phasing of human families.
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Jared C. Roach | Gustavo Glusman | David J. Galas | Katherine S. Pollard | Deepak Srivastava | Leroy Hood | Robert Hubley | Arian F. A. Smit | Alisha K. Holloway | Denise E. Mauldin | L. Hood | J. Roach | K. Pollard | D. Galas | A. Smit | D. Srivastava | R. Hubley | V. Garg | Vidu Garg | Stephen Z. Montsaroff | A. K. Holloway | G Glusman | Gwênlyn Glusman
[1] Leon W. Cohen,et al. Conference Board of the Mathematical Sciences , 1963 .
[2] V. Bansal,et al. The importance of phase information for human genomics , 2011, Nature Reviews Genetics.
[3] Zhaohui S. Qin,et al. A comparison of phasing algorithms for trios and unrelated individuals. , 2006, American journal of human genetics.
[4] P. Shannon,et al. Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing , 2010, Science.
[5] E. Wijsman. A deductive method of haplotype analysis in pedigrees. , 1987, American journal of human genetics.
[6] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[7] Peter Donnelly,et al. A comparison of bayesian methods for haplotype reconstruction from population genotype data. , 2003, American journal of human genetics.
[8] Andrew C. Adey,et al. Haplotype-resolved genome sequencing of a Gujarati Indian individual , 2011, Nature Biotechnology.
[9] Xin Li. Haplotype Inference from Pedigree Data and Population Data , 2010 .
[10] I. Amit,et al. Comprehensive mapping of long range interactions reveals folding principles of the human genome , 2011 .
[11] D. Waggoner. Mechanisms of disease: epigenesis. , 2007, Seminars in pediatric neurology.
[12] Russell Schwartz,et al. Algorithmic strategies for the single nucleotide polymorphism haplotype assembly problem , 2002, Briefings Bioinform..
[13] D. Qian,et al. Minimum-recombinant haplotyping in pedigrees. , 2002, American journal of human genetics.
[14] J. Roach,et al. Pairwise end sequencing: a unified approach to genomic mapping and sequencing. , 1995, Genomics.
[15] Elizabeth A. Thompson,et al. Statistical inference from genetic data on pedigrees , 2003 .
[16] A. Whittemore,et al. Allele-sharing among affected relatives: non-parametric methods for identifying genes , 2001, Statistical methods in medical research.
[17] M. Simon,et al. Analysis of the 1.1-Mb Human α/δ T-Cell Receptor Locus with Bacterial Artificial Chromosome Clones , 1997 .
[18] Timothy B. Stockwell,et al. The Diploid Genome Sequence of an Individual Human , 2007, PLoS biology.
[19] Genomics: No half measures for haplotypes , 2011, Nature Reviews Genetics.
[20] K. P. Donnelly,et al. The probability that related individuals share some section of genome identical by descent. , 1983, Theoretical population biology.
[21] Robert M. Plenge,et al. Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis , 2008, PLoS genetics.
[22] T. Niu. Algorithms for inferring haplotypes , 2004, Genetic epidemiology.
[23] Stephen R Quake,et al. Whole-genome molecular haplotyping of single cells , 2011, Nature Biotechnology.