Skip to content

Latest commit

 

History

History
125 lines (85 loc) · 5.82 KB

README.rst

File metadata and controls

125 lines (85 loc) · 5.82 KB
Raw

Tombo Summary

travis_badge

Tombo is a suite of tools primarily for the identification of modified nucleotides from nanopore sequencing data.

Tombo also provides tools for the analysis and visualization of raw nanopore signal.

Installation

bioconda_badge pypi_badge

Basic tombo installation (python 2.7 and 3.4+ support)

# install via bioconda environment
conda install -c bioconda ont-tombo

# or install pip package (numpy install required before tombo for cython optimization)
pip install numpy
pip install ont-tombo[full]

Quick Start

This quick start guides the steps to perform some common modified base detection analyses using the Tombo command line interface.

The first step in any Tombo analysis is to re-squiggle (raw signal to reference sequence alignment) raw nanopore reads. This creates an index and stores the information necessary to perform downstream analyses.

In this example, an E. coli sample is tested for dam and dcm methylation (CpG model also available for human analysis). Using these results, raw signal is plotted at the most significantly modified dcm positions and the dam modified base predictions are output to a wiggle file for use in downstream processing or visualization in a genome browser.

tombo resquiggle path/to/fast5s/ genome.fasta --processes 4 --num-most-common-errors 5
tombo detect_modifications alternative_model --fast5-basedirs path/to/fast5s/ \
    --statistics-file-basename native.e_coli_sample \
    --alternate-bases dam dcm --processes 4

# plot raw signal at most significant dcm locations
tombo plot most_significant --fast5-basedirs path/to/fast5s/ \
    --statistics-filename native.e_coli_sample.dcm.tombo.stats \
    --plot-standard-model --plot-alternate-model dcm \
    --pdf-filename sample.most_significant_dcm_sites.pdf

# produces wig file with estimated fraction of modified reads at each valid reference site
tombo text_output browser_files --statistics-filename native.e_coli_sample.dam.tombo.stats \
    --file-types dampened_fraction --browser-file-basename native.e_coli_sample.dam
# also produce successfully processed reads coverage file for reference
tombo text_output browser_files --fast5-basedirs path/to/fast5s/ \
    --file-types coverage --browser-file-basename native.e_coli_sample

While motif models (CpG, dcm and dam; most accurate) and all-context specific alternate base models (5mC and 6mA; more accurate) are preferred, Tombo also allows users to investigate other or even unknown base modifications.

Here are two example commands running the de_novo method (detect deviations from expected cannonical signal levels) and the level_sample_compare method (detect deviation in signal levels between two samples of interest; works best with high coverage).

tombo detect_modifications de_novo --fast5-basedirs path/to/fast5s/ \
    --statistics-file-basename sample.de_novo_detect --processes 4
tombo text_output browser_files --statistics-filename sample.de_novo_detect.tombo.stats \
    --browser-file-basename sample.de_novo_detect --file-types dampened_fraction

tombo detect_modifications level_sample_compare --fast5-basedirs path/to/fast5s/ \
    --control-fast5-basedirs path/to/control/fast5s/ --minimum-test-reads 50 \
    --processes 4 --statistics-file-basename sample.level_samp_comp_detect
tombo text_output browser_files --statistics-filename sample.level_samp_comp_detect.tombo.stats \
    --browser-file-basename sample.level_samp_comp_detect --file-types statistic
See more complete tutorials on the documentation page.

RNA

All Tombo commands work for direct RNA nanopore reads as well, but a transcriptome reference sequence must be provided for spliced transcripts.

Tips for processing direct RNA reads within the Tombo framework can be found in the RNA section of the detailed Tombo documentation.

Further Documentation

Run tombo -h to see all Tombo command groups and run tombo [command-group] -h to see all commands within each group.

Detailed documentation for all Tombo commands and algorithms can be found on the tombo documentation page.

Citation

Stoiber, M.H. et al. De novo Identification of DNA Modifications Enabled by Genome-Guided Nanopore Signal Processing. bioRxiv (2016).

http://biorxiv.org/content/early/2017/04/10/094672

Known Issues

  • The Tombo conda environment (especially with python 2.7) may have installation issues.

    • Tombo works best in python 3.4+, so many problems can be solved by upgrading python.

    • If installed using conda:

      • Ensure the most recent version of conda is installed (conda update -n root conda).
      • It is recommended to set conda channels as described for bioconda.
      • Run conda update --all.

    • In python 2.7 there is an issue with the conda scipy.stats package. Down-grading to version 0.17 fixes this issue.

    • In python 2.7 there is an issue with the conda h5py package. Down-grading to version <=2.7.0 fixes this issue.