| scholarly article | Q13442814 |
| P50 | author | Noah Rosenberg | Q7045447 |
| P2093 | author name string | Chaolong Wang | |
| Lucy Huang | |||
| P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
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| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | statistics | Q12483 |
| imputation | Q1660484 | ||
| P304 | page(s) | 692-698 | |
| P577 | publication date | 2009-10-22 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | The relationship between imputation error and statistical power in genetic association studies in diverse populations | |
| P478 | volume | 85 |
| Q30371643 | A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records |
| Q36154414 | A coalescent model for genotype imputation. |
| Q37422525 | A generic coalescent-based framework for the selection of a reference panel for imputation |
| Q37282688 | A genome-wide association study for somatic cell score using the Illumina high-density bovine beadchip identifies several novel QTL potentially related to mastitis susceptibility |
| Q46032408 | A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. |
| Q96302889 | A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness |
| Q55157765 | A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. |
| Q30836450 | Accuracy of imputation to whole-genome sequence data in Holstein Friesian cattle |
| Q33890017 | Assessing accuracy of genotype imputation in American Indians |
| Q34614279 | Assessing the impact of differential genotyping errors on rare variant tests of association |
| Q35546078 | Assessing the impact of non-differential genotyping errors on rare variant tests of association |
| Q34505607 | Assessment of genotype imputation performance using 1000 Genomes in African American studies |
| Q30828110 | Effective filtering strategies to improve data quality from population-based whole exome sequencing studies. |
| Q30879655 | Evaluating the concordance between sequencing, imputation and microarray genotype calls in the GAW18 data. |
| Q34300842 | Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes |
| Q36068167 | Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants |
| Q93055793 | Functional validity, role, and implications of heavy alcohol consumption genetic loci |
| Q91897339 | Generating High Density, Low Cost Genotype Data in Soybean [Glycine max (L.) Merr.]. |
| Q57295893 | Genetic variation in the locus is associated with erectile dysfunction |
| Q37725795 | Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation |
| Q34514955 | Genome-wide association of breast cancer: composite likelihood with imputed genotypes |
| Q34817128 | Genome-wide association studies in diverse populations |
| Q28296883 | Genomics: In search of rare human variants |
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| Q34118461 | Multistudy fine mapping of chromosome 2q identifies XRCC5 as a chronic obstructive pulmonary disease susceptibility gene |
| Q47304007 | Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies |
| Q35720540 | Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate |
| Q50546663 | PreCimp: Pre-collapsing imputation approach increases imputation accuracy of rare variants in terms of collapsed variables. |
| Q30793085 | Predicting HLA alleles from high-resolution SNP data in three Southeast Asian populations |
| Q34945544 | Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification |
| Q28081028 | Strategies for Imputing and Analyzing Rare Variants in Association Studies |
| Q48272232 | Strategies for phasing and imputation in a population isolate. |
| Q37766201 | The genome-wide association study--a new era for common polygenic disorders |
| Q30841937 | Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond |
| Q37398707 | Variation at HLA-DRB1 is associated with resistance to enteric fever |
| Q30362046 | Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. |
| Q42784270 | Windfalls and pitfalls: Applications of population genetics to the search for disease genes. |
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