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Penguin: A Tool for Predicting Pseudouridine Sites in Direct RNA Nanopore Sequencing Data

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Penguin

Penguin: A Tool for Predicting Pseudouridine Sites in Direct RNA Nanopore Sequencing Data

Getting Started and pre-requisites

The following softwares and modules should be installed before using Penguin

python 3.6.10

minimpa2 (https://github.com/lh3/minimap2)

Nanopolish (https://github.com/jts/nanopolish)

samtools (http://www.htslib.org/)

numpy 1.18.1

pandas 1.0.1

sklearn 0.22.2.post1

tensorflow 2.0.0

keras 2.3.1 (using Tensorflow backend)

Running Penguin:

In order to run Penguin, the user has do the following:

1- Ensure that the bedfile in the same path where penguin main.py file exists: 2- Run the following python command:

python main.py -r ref.fa -f reads.fastq

Where the penguin tool needs the following two inputs files when running it:

  • A reference Genome file (ref.fa)
  • The fastq reads file (reads.fastq)

Note:

  • The user should enter the bed file name with the absolute path and extension

  • The user should include the fast5 files folder (fast5_files) from which reads.fastq file was generated in the same path of main.py

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