AIMC Topic: Models, Genetic

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LogLoss-BERAF: An ensemble-based machine learning model for constructing highly accurate diagnostic sets of methylation sites accounting for heterogeneity in prostate cancer.

PloS one
Although modern methods of whole genome DNA methylation analysis have a wide range of applications, they are not suitable for clinical diagnostics due to their high cost and complexity and due to the large amount of sample DNA required for the analys...

Detecting gene-gene interactions for complex quantitative traits using generalized fuzzy classification.

BMC bioinformatics
BACKGROUND: Quantitative traits or continuous outcomes related to complex diseases can provide more information and therefore more accurate analysis for identifying gene-gene and gene- environment interactions associated with complex diseases. Multif...

CEA: Combination-based gene set functional enrichment analysis.

Scientific reports
Functional enrichment analysis is a fundamental and challenging task in bioinformatics. Most of the current enrichment analysis approaches individually evaluate functional terms and often output a list of enriched terms with high similarity and redun...

Combinatorial Scoring of Phylogenetic Trees and Networks Based on Homoplasy-Free Characters.

Journal of computational biology : a journal of computational molecular cell biology
Construction of phylogenetic trees and networks for extant species from their characters represents one of the key problems in phylogenomics. While solution to this problem is not always uniquely defined and there exist multiple methods for tree/netw...

A deep convolutional neural network approach for predicting phenotypes from genotypes.

Planta
Deep learning is a promising technology to accurately select individuals with high phenotypic values based on genotypic data. Genomic selection (GS) is a promising breeding strategy by which the phenotypes of plant individuals are usually predicted b...

Establishment of a SVM classifier to predict recurrence of ovarian cancer.

Molecular medicine reports
Gene expression data using retrieved ovarian cancer (OC) samples were used to identify genes of interest and a support vector machine (SVM) classifier was subsequently established to predict the recurrence of OC. Three datasets (GSE17260, GSE44104 an...

Data mining of the cancer-related lncRNAs GO terms and KEGG pathways by using mRMR method.

Mathematical biosciences
LncRNAs plays an important role in the regulation of gene expression. Identification of cancer-related lncRNAs GO terms and KEGG pathways is great helpful for revealing cancer-related functional biological processes. Therefore, in this study, we prop...

Class Balanced Multifactor Dimensionality Reduction to Detect Gene-Gene Interactions.

IEEE/ACM transactions on computational biology and bioinformatics
Detecting gene-gene interactions in single-nucleotide polymorphism data is vital for understanding disease susceptibility. However, existing approaches may be limited by the sample size in case-control studies. Herein, we propose a balance approach f...

Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk.

Nature genetics
Key challenges for human genetics, precision medicine and evolutionary biology include deciphering the regulatory code of gene expression and understanding the transcriptional effects of genome variation. However, this is extremely difficult because ...

Deep learning models for bacteria taxonomic classification of metagenomic data.

BMC bioinformatics
BACKGROUND: An open challenge in translational bioinformatics is the analysis of sequenced metagenomes from various environmental samples. Of course, several studies demonstrated the 16S ribosomal RNA could be considered as a barcode for bacteria cla...