AIMC Topic: Models, Genetic

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Marker effects and heritability estimates using additive-dominance genomic architectures via artificial neural networks in Coffea canephora.

PloS one
Many methodologies are used to predict the genetic merit in animals and plants, but some of them require priori assumptions that may increase the complexity of the model. Artificial neural network (ANN) has advantage to not require priori assumptions...

Genetic prediction of ICU hospitalization and mortality in COVID-19 patients using artificial neural networks.

Journal of cellular and molecular medicine
There is an unmet need of models for early prediction of morbidity and mortality of Coronavirus disease-19 (COVID-19). We aimed to a) identify complement-related genetic variants associated with the clinical outcomes of ICU hospitalization and death,...

Modeling CRISPR gene drives for suppression of invasive rodents using a supervised machine learning framework.

PLoS computational biology
Invasive rodent populations pose a threat to biodiversity across the globe. When confronted with these invaders, native species that evolved independently are often defenseless. CRISPR gene drive systems could provide a solution to this problem by sp...

GCAEMDA: Predicting miRNA-disease associations via graph convolutional autoencoder.

PLoS computational biology
microRNAs (miRNAs) are small non-coding RNAs related to a number of complicated biological processes. A growing body of studies have suggested that miRNAs are closely associated with many human diseases. It is meaningful to consider disease-related m...

Enhancing breakpoint resolution with deep segmentation model: A general refinement method for read-depth based structural variant callers.

PLoS computational biology
Read-depths (RDs) are frequently used in identifying structural variants (SVs) from sequencing data. For existing RD-based SV callers, it is difficult for them to determine breakpoints in single-nucleotide resolution due to the noisiness of RD data a...

Spatial rank-based multifactor dimensionality reduction to detect gene-gene interactions for multivariate phenotypes.

BMC bioinformatics
BACKGROUND: Identifying interaction effects between genes is one of the main tasks of genome-wide association studies aiming to shed light on the biological mechanisms underlying complex diseases. Multifactor dimensionality reduction (MDR) is a popul...

VEGA is an interpretable generative model for inferring biological network activity in single-cell transcriptomics.

Nature communications
Deep learning architectures such as variational autoencoders have revolutionized the analysis of transcriptomics data. However, the latent space of these variational autoencoders offers little to no interpretability. To provide further biological ins...

Evolutionarily informed machine learning enhances the power of predictive gene-to-phenotype relationships.

Nature communications
Inferring phenotypic outcomes from genomic features is both a promise and challenge for systems biology. Using gene expression data to predict phenotypic outcomes, and functionally validating the genes with predictive powers are two challenges we add...

Genetic dissection of complex traits using hierarchical biological knowledge.

PLoS computational biology
Despite the growing constellation of genetic loci linked to common traits, these loci have yet to account for most heritable variation, and most act through poorly understood mechanisms. Recent machine learning (ML) systems have used hierarchical bio...

ReFeaFi: Genome-wide prediction of regulatory elements driving transcription initiation.

PLoS computational biology
Regulatory elements control gene expression through transcription initiation (promoters) and by enhancing transcription at distant regions (enhancers). Accurate identification of regulatory elements is fundamental for annotating genomes and understan...