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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HiContacts provides a collection of tools to analyse and visualize Hi-C datasets imported in R by HiCExperiment.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
library(HiCExperiment)
library(HiContacts)
library(HiContactsData)
# Import Hi-C matrix
cool_file <- HiContactsData('yeast_wt', format = 'cool')
hic <- import(cool_file, format = 'cool')
# Perform matrix arithmetic
hic_detrended <- detrend(hic)
hic_smooth <- despeckle(hic)
# Plot contact map
plotMatrix(hic_smooth, use.scores = 'balanced.despeckled')
Input: A HiCExperiment object.
Output: Detrended, smoothed, or merged contact maps and their corresponding plots.
library(HiCExperiment)
library(HiContacts)
library(HiContactsData)
mcool_file <- HiContactsData('yeast_wt', format = 'mcool')
hic <- import(mcool_file, format = 'mcool', resolution = 1000)
# Calculate cis-trans ratios
ratios <- cisTransRatio(hic)
# Compute distance decay P(s) curves
ps <- distanceLaw(hic)
Input: A HiCExperiment object, optionally with an associated pairs file.
Output: A tibble of cis-trans ratios and distance decay P(s) curves.
library(HiCExperiment)
library(HiContacts)
library(HiContactsData)
mcool_file <- HiContactsData('yeast_wt', format = 'mcool')
hic <- import(mcool_file, format = 'mcool', resolution = 16000)
# Map chromosome compartments
hic <- getCompartments(hic, chromosomes = c('XV', 'XVI'))
# Compute insulation scores and borders
hic <- refocus(hic, 'II:1-300000') |>
zoom(resolution = 1000) |>
getDiamondInsulation(window_size = 8000) |>
getBorders()
Input: A HiCExperiment object.
Output: A HiCExperiment object updated with compartments, insulation scores, and domain borders.
plotMatrix().detrend()), autocorrelating (autocorrelate()), merging (merge()), dividing (divide()), and smoothing (despeckle()).getCompartments()), insulation scores (getDiamondInsulation()), and domain borders (getBorders()).distanceLaw() and plotting them with plotPs() or plotPsSlope().HiContacts.GenomicRanges or IRanges directly.HiCExperiment object imported from .cool, .mcool, .hic, or HiC-Pro files..pairs.gz) should be linked using pairsFile(hic) <- ....'balanced', 'detrended', 'autocorrelated').plotMatrix().despeckle().getDiamondInsulation().getCompartments().'balanced') rather than raw counts for comparative analyses.pairsFile() before running distanceLaw() to avoid approximations in the P(s) curve.rtracklayer::export().distanceLaw() without a pairs file: This results in an approximation warning. Fix by assigning a pairs file to the HiCExperiment object first.scale = 'log10' in plotMatrix() to improve visualization.diffHic: For differential analysis of Hi-C data using biological replicates.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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