Nancy Jean Cox to Software
This is a "connection" page, showing publications Nancy Jean Cox has written about Software.
Connection Strength
1.280
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SCAN: SNP and copy number annotation. Bioinformatics. 2010 Jan 15; 26(2):259-62.
Score: 0.230
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Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. Nat Commun. 2024 Feb 03; 15(1):1016.
Score: 0.154
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FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Res. 2023 01 06; 51(D1):D1300-D1311.
Score: 0.143
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Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs. Bioinformatics. 2023 01 01; 39(1).
Score: 0.143
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MERLIN...and the geneticist's stone? Nat Genet. 2002 Jan; 30(1):3-4.
Score: 0.133
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De novo pattern discovery enables robust assessment of functional consequences of non-coding variants. Bioinformatics. 2019 05 01; 35(9):1453-1460.
Score: 0.111
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Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes. Bioinformatics. 2015 Jan 15; 31(2):187-93.
Score: 0.080
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GEL: a novel genotype calling algorithm using empirical likelihood. Bioinformatics. 2006 Aug 15; 22(16):1942-7.
Score: 0.045
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Rational inferences about departures from Hardy-Weinberg equilibrium. Am J Hum Genet. 2005 Jun; 76(6):967-86.
Score: 0.042
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Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED. Genet Epidemiol. 1984; 1(2):167-70.
Score: 0.038
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Improving the computation efficiency of polygenic risk score modeling: faster in Julia. Life Sci Alliance. 2022 07 18; 5(12).
Score: 0.035
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Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet. 1997 Nov; 61(5):1179-88.
Score: 0.025
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Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record. PLoS One. 2017; 12(7):e0175508.
Score: 0.024
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Poly-omic prediction of complex traits: OmicKriging. Genet Epidemiol. 2014 Jul; 38(5):402-15.
Score: 0.020
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Importance sampling. I. Computing multimodel p values in linkage analysis. Am J Hum Genet. 1992 Dec; 51(6):1413-29.
Score: 0.018
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Power and sample size calculations for SNP association studies with censored time-to-event outcomes. Genet Epidemiol. 2012 Sep; 36(6):538-48.
Score: 0.017
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Robust sequence selection method used to develop the FluChip diagnostic microarray for influenza virus. J Clin Microbiol. 2006 Aug; 44(8):2857-62.
Score: 0.011
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Segregation analyses of stuttering. Genet Epidemiol. 1984; 1(3):245-53.
Score: 0.010
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The detection of major loci by segregation and linkage analysis: a simulation study. Genet Epidemiol. 1984; 1(3):285-96.
Score: 0.002