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PQLseq (version 1.2.1)

Efficient Mixed Model Analysis of Count Data in Large-Scale Genomic Sequencing Studies

Description

An efficient tool designed for differential analysis of large-scale RNA sequencing (RNAseq) data and Bisulfite sequencing (BSseq) data in the presence of individual relatedness and population structure. 'PQLseq' first fits a Generalized Linear Mixed Model (GLMM) with adjusted covariates, predictor of interest and random effects to account for population structure and individual relatedness, and then performs Wald tests for each gene in RNAseq or site in BSseq.

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Version

Install

install.packages('PQLseq')

Monthly Downloads

83

Version

1.2.1

License

GPL (>= 2)

Maintainer

Jiaqiang Zhu

Last Published

June 6th, 2021

Functions in PQLseq (1.2.1)

ExampleBSseq

BSseq example dataset
pqlseq

Fit Generalized Linear Mixed Model with Known Kinship Matrices Through Penalized-quasi Likelihood
ExampleRNAseq

RNAseq example dataset
PQLseq-package

PQLseq