These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
193 related articles for article (PubMed ID: 18492685)
1. MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data. Kato M; Nakamura Y; Tsunoda T Bioinformatics; 2008 Jul; 24(14):1645-6. PubMed ID: 18492685 [TBL] [Abstract][Full Text] [Related]
2. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle. Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735 [TBL] [Abstract][Full Text] [Related]
3. Estimation of haplotype frequencies, linkage-disequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data. Ito T; Chiku S; Inoue E; Tomita M; Morisaki T; Morisaki H; Kamatani N Am J Hum Genet; 2003 Feb; 72(2):384-98. PubMed ID: 12533787 [TBL] [Abstract][Full Text] [Related]
4. Population-genetic nature of copy number variations in the human genome. Kato M; Kawaguchi T; Ishikawa S; Umeda T; Nakamichi R; Shapero MH; Jones KW; Nakamura Y; Aburatani H; Tsunoda T Hum Mol Genet; 2010 Mar; 19(5):761-73. PubMed ID: 19966329 [TBL] [Abstract][Full Text] [Related]
5. An algorithm for inferring complex haplotypes in a region of copy-number variation. Kato M; Nakamura Y; Tsunoda T Am J Hum Genet; 2008 Aug; 83(2):157-69. PubMed ID: 18639202 [TBL] [Abstract][Full Text] [Related]
6. Genotype, haplotype and copy-number variation in worldwide human populations. Jakobsson M; Scholz SW; Scheet P; Gibbs JR; VanLiere JM; Fung HC; Szpiech ZA; Degnan JH; Wang K; Guerreiro R; Bras JM; Schymick JC; Hernandez DG; Traynor BJ; Simon-Sanchez J; Matarin M; Britton A; van de Leemput J; Rafferty I; Bucan M; Cann HM; Hardy JA; Rosenberg NA; Singleton AB Nature; 2008 Feb; 451(7181):998-1003. PubMed ID: 18288195 [TBL] [Abstract][Full Text] [Related]
7. HaplotypeCN: copy number haplotype inference with Hidden Markov Model and localized haplotype clustering. Lin YJ; Chen YT; Hsu SN; Peng CH; Tang CY; Yen TC; Hsieh WP PLoS One; 2014; 9(5):e96841. PubMed ID: 24849202 [TBL] [Abstract][Full Text] [Related]
8. Haplotype phasing and inheritance of copy number variants in nuclear families. Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576 [TBL] [Abstract][Full Text] [Related]
9. Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation. Clark VJ; Dean M Hum Genomics; 2004 Mar; 1(3):195-207. PubMed ID: 15588479 [TBL] [Abstract][Full Text] [Related]
10. Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms. Li SS; Khalid N; Carlson C; Zhao LP Biostatistics; 2003 Oct; 4(4):513-22. PubMed ID: 14557108 [TBL] [Abstract][Full Text] [Related]
11. Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'. Gaunt TR; Rodríguez S; Day IN BMC Bioinformatics; 2007 Nov; 8():428. PubMed ID: 17980034 [TBL] [Abstract][Full Text] [Related]
12. An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history. Gaunt TR; Rodriguez S; Guthrie PA; Day IN Hum Mutat; 2010 Apr; 31(4):414-20. PubMed ID: 20077501 [TBL] [Abstract][Full Text] [Related]
13. A haplotype sharing method for determining the relative age of SNP alleles. de Vries AR; te Meerman GJ Hum Hered; 2010; 69(1):52-9. PubMed ID: 19797909 [TBL] [Abstract][Full Text] [Related]