A simple tool designed to visualize the features that distinguish between two groups of ONT data at the site level. It supports 4 re-squiggle program(tombo resquiggle/f5c resquiggle/f5c eventalign/move_table).
Project description
nanoCEM
The nanopore current events magnifier (nanoCEM
) is a python command line to facilitate the analysis of DNA/RNA modification sites by visualizing statistical features of current events.
NanoCEM can be used to showcase high confidence sites and observe the difference based on the modification sample and the low or no modification sample.
It supports two re-squiggle pipeline(Tombo
and f5c
) and support R9
and R10
.
If you want to view single read signal or raw signal, Squigualiser is recommended.
Installation
Before pip install, make sure you have installed the samtools
(>=1.16) , f5c
(>=1.4), slow5tools
(>=1.1.0) and minimap2
(>=2.17),
conda install samtools=1.16 minimap2 f5c=1.4 slow5tools -c conda-forge -c bioconda
To install the latest nanoCEM
pip install nanoCEM
And install from the resource
git clone https://github.com/lrslab/nanoCEM.git
cd nanoCEM/
pip install .
To install nanoCEM from docker,
docker pull zhihaguo/nanocem_env
To check the version of nanoCEM, run:
pip list | grep nanoCEM
Solutions for some potential environment problem
Although it does not affect the functionality, the issue of possible missing header files caused by samtools installation by conda can be resolved with the following command.
conda install -c conda-forge ncurses
The potential vbz format compression issue when reading fast5 files.
conda install -c bioconda ont_vbz_hdf_plugin
Data release
For the data we used and related commands in our paper, please view our wiki
Documents
Full documentation is available at https://nanocem.readthedocs.io/
Workflow
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