epigraHMM is a
Bioconductor package that provides set of tools to flexibly analyze data
from a wide range of high-throughput epigenomic assays (ChIP-seq,
ATAC-seq, DNase-seq, etc.) in an end-to-end pipeline.
The official page of epigraHMM is the Bioconductor landing page of its
release
(or
devel)
version. This github page is
simply used for issue tracking and development.
Background
A fundamental task in the analysis of data resulting from epigenomic
sequencing assays is the detection of genomic regions with significant
or differential sequencing read enrichment. epigraHMM provides set of
tools to flexibly analyze data from a wide range of high-throughput
epigenomic assays (ChIP-seq, ATAC-seq, DNase-seq, etc.) in an end-to-end
pipeline. It includes functionalities for data pre-processing,
normalization, consensus and differential peak detection, as well as
data visualization. In differential analyses, epigraHMM can detect
differential peaks across either multiple conditions of a single
epigenomic mark (differential peak calling) or across multiple
epigenomic marks from a single condition (genomic segmentation). The
data pre-processing steps are heavily integrated with other Bioconductor
packages and allow the user to transform sequencing/alignment files into
count matrices that are suitable for the final analysis of the data.
The current implementation is optimized for genome-wide analyses of
epigenomic data and is efficient for the analysis under multi-sample
multiple-condition settings, as well as consensus peak calling in
multi-sample single-condition settings. epigraHMM uses two modified
versions of hidden Markov models (HMM) that are robust to the diversity
of peak profiles found in epigenomic data and are particularly useful
for epigenomic marks that exhibit short and broad peaks. Analyses can be
adjusted for possible technical artifacts present in the data and for
input control experiments, if available. Results from the peak calling
algorithms can be assessed using some of the available tools for
visualization that allow the inspection of detected peaks and read
counts.
Installation
You can install the official release version of epigraHMM from
Bioconductor
with:
A
vignette
of epigraHMM with an overview of the package and its functionalities
is available. Users can build the vignette during the installation
process with the option build_vignettes = TRUE in the command above.
The
epigraHMMpackageepigraHMM is a Bioconductor package that provides set of tools to flexibly analyze data from a wide range of high-throughput epigenomic assays (ChIP-seq, ATAC-seq, DNase-seq, etc.) in an end-to-end pipeline.
The official page of
epigraHMMis the Bioconductor landing page of its release (or devel) version. This github page is simply used for issue tracking and development.Background
A fundamental task in the analysis of data resulting from epigenomic sequencing assays is the detection of genomic regions with significant or differential sequencing read enrichment.
epigraHMMprovides set of tools to flexibly analyze data from a wide range of high-throughput epigenomic assays (ChIP-seq, ATAC-seq, DNase-seq, etc.) in an end-to-end pipeline. It includes functionalities for data pre-processing, normalization, consensus and differential peak detection, as well as data visualization. In differential analyses,epigraHMMcan detect differential peaks across either multiple conditions of a single epigenomic mark (differential peak calling) or across multiple epigenomic marks from a single condition (genomic segmentation). The data pre-processing steps are heavily integrated with other Bioconductor packages and allow the user to transform sequencing/alignment files into count matrices that are suitable for the final analysis of the data.The current implementation is optimized for genome-wide analyses of epigenomic data and is efficient for the analysis under multi-sample multiple-condition settings, as well as consensus peak calling in multi-sample single-condition settings.
epigraHMMuses two modified versions of hidden Markov models (HMM) that are robust to the diversity of peak profiles found in epigenomic data and are particularly useful for epigenomic marks that exhibit short and broad peaks. Analyses can be adjusted for possible technical artifacts present in the data and for input control experiments, if available. Results from the peak calling algorithms can be assessed using some of the available tools for visualization that allow the inspection of detected peaks and read counts.Installation
You can install the official release version of
epigraHMMfrom Bioconductor with:A vignette of
epigraHMMwith an overview of the package and its functionalities is available. Users can build the vignette during the installation process with the optionbuild_vignettes = TRUEin the command above.