ArticleGenes & genomics2021
Towards fine-scale population stratification modeling based on kernel principal component analysis and random forest.
Article in Genes & genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPopulation stratification modeling is essential in Genome-Wide Association Studies.
objectiveIn this paper, we aim to build a fine-scale population stratification model to efficiently infer individual genetic ancestry.
methodsKernel Principal Component Analysis (PCA) and random forest are adopted to build the population stratification model, together with parameter optimization. We explore different PCA methods, including standard PCA and kernel PCA to extract relevant features from the genotype data that is transformed by vcf2geno, a pipeline from LASER software. These extracted features are fed into a random forest for ensemble learning. Parameter tuning is performed to jointly find the optimal number of principal components, kernel function for PCA and parameters of the random forest.
resultsExperiments based on HGDP dataset show that kernel PCA with Sigmoid function and Gaussian function can achieve higher prediction accuracy than the standard PCA. Compared to standard PCA with the two principal components, the accuracy by using KPCA-Sigmoid with the optimal number of principal components can achieve around 100% and 200% improvement for East Asian and European populations, respectively.
conclusionWith the optimal parameter configuration on both PCA and random forest, our proposed method can infer the individual genetic ancestry more accurately, given their variants.
Indexed as
Identifiers
34097252What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.