The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
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This package is a implementation of biclustering ensemble method MoSBi (Molecular signature Identification from Biclustering). MoSBi provides standardized interfaces for biclustering results and can combine their results with a multi-algorithm ensemble approach to compute robust ensemble biclusters on molecular omics data. This is done by computing similarity networks of biclusters and filtering for overlaps using a custom error model. After that, the louvain modularity it used to extract biclus
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Run multiple biclustering algorithms on a data matrix, construct a similarity network with an error model, extract robust communities, and generate consensus ensemble biclusters.
library(mosbi)
# 1. Prepare data matrix
data(mouse_data)
mouse_data_sub <- mouse_data[c(grep("metabolite_identification", colnames(mouse_data)), grep("^X", colnames(mouse_data)))]
# Simple mock matrix for runnable demonstration
data_matrix <- matrix(rnorm(1000), nrow = 100, ncol = 10)
rownames(data_matrix) <- paste0("M", 1:100)
colnames(data_matrix) <- paste0("S", 1:10)
# 2. Run Biclustering Algorithms
fb <- mosbi::run_fabia(data_matrix)
BCisa <- mosbi::run_isa(data_matrix)
BCplaid <- mosbi::run_plaid(data_matrix)
BCqubic <- mosbi::run_qubic(data_matrix)
all_bics <- c(fb, BCisa, BCplaid, BCqubic)
# 3. Compute Bicluster Similarity Network with Error Model
bic_net <- mosbi::bicluster_network(all_bics, data_matrix, n_randomizations = 5, MARGIN = "both", metric = 4)
# 4. Extract Louvain Communities
coms <- mosbi::get_louvain_communities(bic_net, min_size = 3, bics = all_bics)
# 5. Generate Consensus Ensemble Biclusters
ensemble_bicluster_list <- mosbi::ensemble_biclusters(coms, all_bics, data_matrix, row_threshold = 0.1, col_threshold = 0.1)
Input: A numeric data matrix; Output: A list of robust ensemble biclusters.
run_fabia, ISA via run_isa, Plaid via run_plaid, QUBIC via run_qubic) and combine their results.bicluster_network.get_louvain_communities and generate consensus ensemble biclusters via ensemble_biclusters.biclust or fabia can be used directly.data_matrix in the vignette derived from mouse_data using log2 and z-score normalization).bicluster_network.bicluster_network.bicluster_network.bicluster_network.bicluster_network.get_louvain_communities.colhistogram and rowhistogram (or a helper like bicluster_histo).plot_edge_dist = TRUE in bicluster_network.plot or plot_algo_network to inspect how different algorithms contribute to communities.get_louvain_communities with a min_size that is too high, resulting in zero saved communities. Fix: Lower min_size (e.g., to 3).biclust for running individual biclustering algorithms like Plaid.fabia for Fabia biclustering.QUBIC for QUBIC biclustering.isa2 for ISA biclustering.아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
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The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
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This tool uses the label-tree function from HyPhy to annotate a phylogenetic tree. It allows users to select a subset of leaves using either a regular expression or a list of sequence names, and then apply a specified label to these selecte
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This package provides a client for the Bioconductor AnnotationHub web resource. The AnnotationHub web resource provides a central location where genomic files (e.g., VCF, bed, wig) and other resources from standard locations (e.g., UCSC, En
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apeglm provides Bayesian shrinkage estimators for effect sizes for a variety of GLM models, using approximation of the posterior for individual coefficients.
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ASURAT is a software for single-cell data analysis. Using ASURAT, one can simultaneously perform unsupervised clustering and biological interpretation in terms of cell type, disease, biological process, and signaling pathway activity. Inputting a single-cell RNA-seq data and knowledge-based databases, such as Cell Ontology, Gene Ontology, KEGG, etc., ASURAT transforms gene expression tables into original multivariate tables, termed sign-by-sample matrices (SSMs).
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AUCell allows to identify cells with active gene sets (e.g. signatures, gene modules...) in single-cell RNA-seq data. AUCell uses the "Area Under the Curve" (AUC) to calculate whether a critical subset of the input gene set is enriched with
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