ReferencesΒΆ

[Dempster1977]Dempster, A. P., Laird, N. M., Rubin D., (1977), ‘Maximum likelihood from incomplete data via the EM algorithm.’ J of the Royal Stat Soc B 39: 1-38.
[Excoffier1995]Excoffier L, Slatkin M (1995) ‘Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.’ Molecular Biology and Evolution 12: 921–927.
[Nicol2009]Nicol JW, Helt GA, Blanchard SG Jr, Raja A, Loraine AE (2009) The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets. Bioinformatics. 25(20):2730-1. PubMed PMID: 19654113; PubMed Central PMCID: PMC2759552
[Nielsen1998]Nielsen D, Ehm M, Weir BS (1998) ‘Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus.’ Am J Hum Genet 63: 1531–1540.
[Weir1996]Weir BS (1996) ‘Genetic Data Analysis II.’ Sinauer Associates.
[Zaykin2000]Zaykin DV, Nielsen DM (2000) ‘Hardy-Weinberg disequilibrium (HWD) fine mapping for case-control samples.’ Am J Hum Genet 67: 1238(S).
[Zaykin2001]Zaykin DV, Ehm, MG, Weir BS (2001) ‘Evaluating new haplotyping methods for predicting clinical response using dense maps of single nucleotide polymorphisms (SNPs).’ Work in progress. Presented at Bioinformatics Seminar Series, Research Triangle Institute, NC.