Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 54 checked references that resolve
resolves10.1016/j.cub.2016.01.065Individual Identifiability Predicts Population Identifiability in Forensic Microsatellite Markers
resolves10.1086/377588Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas
resolves10.1073/pnas.97.1.262Knowledge-based analysis of microarray gene expression data by using support vector machines
resolves10.1007/s00439-016-1740-0The Y chromosome as the most popular marker in genetic genealogy benefits interdisciplinary research
resolves10.1371/journal.pone.0062005Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals
resolves10.1007/s11517-021-02476-xHybrid gene selection approach using XGBoost and multi-objective genetic algorithm for cancer classification
resolves10.1136/ard.2006.054304A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients
resolves10.1016/j.fsigen.2009.03.002Inferring ethnicity using 15 autosomal STR loci—Comparisons among populations of similar and distinctly different physical traits
resolves10.1016/j.eswa.2010.09.112Integrating genetic algorithm and decision tree learning for assistance in predicting in vitro fertilization outcomes
resolves10.1016/j.forsciint.2005.11.013Population structure of Y chromosome SNP haplogroups in the United States and forensic implications for constructing Y chromosome STR databases
resolves10.1002/gepi.22427Random effect based tests for multinomial logistic regression in genetic association studies
resolves10.1016/j.jare.2020.11.006A risk prediction model of gene signatures in ovarian cancer through bagging of GA-XGBoost models
resolves10.1038/nature06742Genotype, haplotype and copy-number variation in worldwide human populations
resolves10.1086/302825The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data
resolves10.1093/bioinformatics/btw075Trinculo: Bayesian and frequentist multinomial logistic regression for genome-wide association studies of multi-category phenotypes
resolves10.1016/j.eswa.2010.07.053Gene selection and sample classification on microarray data based on adaptive genetic algorithm/k-nearest neighbor method
resolves10.2174/1386207013330733Gene Assessment and Sample Classification for Gene Expression Data Using a Genetic Algorithm / k-nearest Neighbor Method
resolves10.1038/ejhg.2014.134Copy number variations and genetic admixtures in three Xinjiang ethnic minority groups
resolves10.3390/cells8040306Comparing the Utility of Mitochondrial and Nuclear DNA to Adjust for Genetic Ancestry in Association Studies
resolves10.1093/gbe/evu250Extensive Copy Number Variations in Admixed Indian Population of African Ancestry: Potential Involvement in Adaptation
resolves10.1038/tpj.2010.56k-Nearest neighbor models for microarray gene expression analysis and clinical outcome prediction
resolves10.1007/s00414-010-0472-2PopAffiliator: online calculator for individual affiliation to a major population group based on 17 autosomal short tandem repeat genotype profile
resolves10.1002/elps.201200621Development of a novel forensic <scp>STR</scp> multiplex for ancestry analysis and extended identity testing
resolves10.1002/elps.201400095“New turns from old STaRs”: Enhancing the capabilities of forensic short tandem repeat analysis
resolves10.1002/ajpa.20765Genetic admixture, relatedness, and structure patterns among Mexican populations revealed by the Y‐chromosome
resolves10.1086/380416Informativeness of Genetic Markers for Inference of Ancestry*
resolves10.1007/s00125-014-3256-2Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification
resolves10.1002/ajpa.21194The genetic structure of populations from Haiti and Jamaica reflect divergent demographic histories
resolves10.1111/acer.12364Association Between Copy Number Variation Losses and Alcohol Dependence Across <scp>A</scp>frican <scp>A</scp>merican and <scp>E</scp>uropean <scp>A</scp>merican Ethnic Groups
resolves10.1016/j.procs.2015.03.178Gene Expression Data Classification Using Support Vector Machine and Mutual Information-based Gene Selection
resolves10.1186/1752-0509-7-119Decision tree-based method for integrating gene expression, demographic, and clinical data to determine disease endotypes
The 16 references without a DOI — listed, not checked
no DOI — not checkedMultinomial logistic regression approach to haplotype association analysis in populationbased case-control studies
no DOI — not checkedPerformance of ancestry-informative SNP and microhaplotype markers
no DOI — not checkedref14
no DOI — not checkedApplications of Support Vector Machine (SVM) Learning in Cancer Genomics
no DOI — not checkedPerformance Evaluation XGBoost in Handling Missing Value on Classification of Hepatocellular Carcinoma Gene Expression Data
no DOI — not checkedInferring ethnicity from mitochondrial DNA sequence
no DOI — not checkedXGBoost-based and tumor-immune characterized gene signature for the prediction of metastatic status in breast cancer
no DOI — not checkedGene expression value prediction based on XGBoost algorithm
no DOI — not checkedHierarchical Naive Bayes for genetic association studies
no DOI — not checkedref44
no DOI — not checkedref53
no DOI — not checkedGene selection by sample classification using k nearest neighbor and metaheuristic algorithms
no DOI — not checkedref59
no DOI — not checkedref60
no DOI — not checkedref62
no DOI — not checkedForensic autosomal short tandem repeats and their potential association with phenotype
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