Use modifications detection output (from kineticsTools using PacBio sequencing data; or from DeepSignal using Nanopore data) to filter out potential false positives and analyze the distribution of DNA modifications in the genome assembly provided. Aligned Illumina sequencing data (bam files) can also be used for analysis.
Package details |
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Maintainer | |
License | GPL-3 |
Version | 0.0.0.9019 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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