EpiRL learns to detect gene-gene interactions.
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Deep learning models improve cancer detection and typing classification from gene expression data.
New methods detect continuous variation in single-cell data.
Proposes a method to identify relevant genes in autism-related diseases using auxiliary information.
In genome-wide interaction studies, to detect gene-gene interactions, most methods are divided into two folds: single nucleotide polymorphisms (SNP) based and gene-based methods. Basically, the methods based on the gene are more effective than the methods based on a single SNP. Recent years, while the kernel canonical …
Unsupervised two-view learning, or detection of dependencies between two paired data sets, is typically done by some variant of canonical correlation analysis (CCA). CCA searches for a linear projection for each view, such that the correlations between the projections are maximized. The solution is invariant to any lin…
Bayesian methods detect clusters in noisy data more reliably.
The linking genotype to phenotype is the fundamental aim of modern genetics. We focus on study of links between gene expression data and phenotype data through integrative analysis. We propose three approaches. 1) The inherent complexity of phenotypes makes high-throughput phenotype profiling a very difficult and labor…
Motivation: The rapid growth of diverse biological data allows us to consider interactions between a variety of objects, such as genes, chemicals, molecular signatures, diseases, pathways and environmental exposures. Often, any pair of objects--such as a gene and a disease--can be related in different ways, for example…
A hierarchical community detection method using recursive partitioning.
Paper proposes MLPCD for protein community detection in large PPI networks.
SL2MF predicts synthetic lethality using logistic matrix factorization.
Test assesses if a linear classifier is random or significant.
Estimates target GGM using auxiliary studies with false discovery rate control.
Deep learning detects bifurcations in dynamical systems.
Efficient algorithm for sparse PCA reduces data complexity.
We propose a probabilistic model for interpreting gene expression levels that are observed through single-cell RNA sequencing. In the model, each cell has a low-dimensional latent representation. Additional latent variables account for technical effects that may erroneously set some observations of gene expression leve…
In this study, we tested the interaction effect of multimodal datasets using a novel method called the kernel method for detecting higher order interactions among biologically relevant mulit-view data. Using a semiparametric method on a reproducing kernel Hilbert space (RKHS), we used a standard mixed-effects linear mo…
Motivation: Modelling methods that find structure in data are necessary with the current large volumes of genomic data, and there have been various efforts to find subsets of genes exhibiting consistent patterns over subsets of treatments. These biclustering techniques have focused on one data source, often gene expres…
A new method uses gene interaction networks to predict gene functions.
The widely used genetic pleiotropic analysis of multiple phenotypes are often designed for examining the relationship between common variants and a few phenotypes. They are not suited for both high dimensional phenotypes and high dimensional genotype (next-generation sequencing) data. To overcome these limitations, we …
The paper improves Fisher-Pitman tests for Poisson mixtures, detecting autism-related genes.
VEGN uses graph neural networks to predict disease-causing mutations from genetic variants.
Automated tests detect interactions in unstructured data.
Discovering causal genetic variants from large genetic association studies poses many difficult challenges. Assessing which genetic markers are involved in determining trait status is a computationally demanding task, especially in the presence of gene-gene interactions. A non-parametric Bayesian approach in the form o…
A new method for identifying significant gene subsets improves disease prediction.
Bioinformatics tools have been developed to interpret gene expression data at the gene set level, and these gene set based analyses improve the biologists' capability to discover functional relevance of their experiment design. While elucidating gene set individually, inter gene sets association is rarely taken into co…
New method estimates latent gene expression factors without overlap with known confounders.
Bayesian model learns cell types and gene networks from two data views.
New method expands seed genes to functionally related clusters.
Framework analyzes leaf vein architecture using deep learning and statistical methods.
A new method for joint eQTL mapping and gene network estimation.
New method handles correlated genes for better genomic prediction.
Popular online enrichment analysis tools from the field of molecular systems biology provide users with the ability to submit their experimental results as gene sets for individual analysis. Such queries are kept private, and have never before been considered as a resource for integrative analysis. By harnessing gene s…
VGAE learns gene-disease associations from networks, predicting disease-genes.
Elucidating the genetic basis of human diseases is a central goal of genetics and molecular biology. While traditional linkage analysis and modern high-throughput techniques often provide long lists of tens or hundreds of disease gene candidates, the identification of disease genes among the candidates remains time-con…
TWIST algorithm detects communities in multi-layer networks with tensor decomposition.
We present the extention and application of a new unsupervised statistical learning technique--the Partition Decoupling Method--to gene expression data. Because it has the ability to reveal non-linear and non-convex geometries present in the data, the PDM is an improvement over typical gene expression analysis algorith…
Blind Source Separation (BSS) has proven to be a powerful tool for the analysis of composite patterns in engineering and science. We introduce Convex Analysis of Mixtures (CAM) for separating non-negative well-grounded sources, which learns the mixing matrix by identifying the lateral edges of the convex data scatter p…
Collaborative filtering predicts drug responses from gene expression data.
A novel method selects genes for high-dimensional gene expression data with class imbalance.
Proposes a novel network-based neighborhood regression for biological systems.
The problem of multilabel classification when the labels are related through a hierarchical categorization scheme occurs in many application domains such as computational biology. For example, this problem arises naturally when trying to automatically assign gene function using a controlled vocabularies like Gene Ontol…
Identifying latent structure in large data matrices is essential for exploring biological processes. Here, we consider recovering gene co-expression networks from gene expression data, where each network encodes relationships between genes that are locally co-regulated by shared biological mechanisms. To do this, we de…
Proposes a new signal model for high-dimensional, small-sample-size data.
The method integrates survival constraints into NMF for identifying survival-associated gene clusters.
Microarray cancer gene expression data comprise of very high dimensions. Reducing the dimensions helps in improving the overall analysis and classification performance. We propose two hybrid techniques, Biogeography - based Optimization - Random Forests (BBO - RF) and BBO - SVM (Support Vector Machines) with gene ranki…
Bayesian optimization improves classifier selection for acute infection and mortality.