{
"info": {
"author": "Leighton Pritchard",
"author_email": "leighton.pritchard@hutton.ac.uk",
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"classifiers": [
"Development Status :: 4 - Beta",
"Environment :: Console",
"Intended Audience :: Science/Research",
"License :: OSI Approved :: MIT License",
"Natural Language :: English",
"Operating System :: MacOS :: MacOS X",
"Operating System :: POSIX :: Linux",
"Programming Language :: Python",
"Programming Language :: Python :: 3",
"Programming Language :: Python :: 3.5",
"Programming Language :: Python :: 3.6",
"Topic :: Scientific/Engineering :: Bio-Informatics"
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"description": "# README.md (pyani)\n\n[![pyani PyPi version](https://img.shields.io/pypi/v/pyani.svg \"PyPi version\")](https://pypi.python.org/pypi/pyani)\n[![pyani licence](https://img.shields.io/pypi/l/pyani.svg \"PyPi licence\")](https://github.com/widdowquinn/pyani/blob/master/LICENSE)\n[](https://travis-ci.org/widdowquinn/pyani/branches)\n[](https://codecov.io/github/widdowquinn/pyani)\n[](https://hub.docker.com/r/leightonpritchard/average_nucleotide_identity)\n\n\n\n- [Overview](#overview)\n- [Installation](#installation)\n- [Docker images](#docker-images)\n- [Testing `pyani`](#testing-pyani)\n- [Running `pyani`](#running-pyani)\n - [Script: `average_nucleotide_identity.py`](#script-a-nameaverage_nucleotide_identitypyaverage_nucleotide_identitypya)\n - [Script: `genbank_get_genomes_by_taxon.py`](#script-a-namegenbank_get_genomes_by_taxonpygenbank_get_genomes_by_taxonpya)\n- [DEPENDENCIES](#dependencies)\n - [For ANI analysis](#for-ani-analysis)\n - [For graphical output](#for-graphical-output)\n- [Method and Output Description](#method-and-output-description)\n - [Average Nucleotide Identity (ANI)](#average-nucleotide-identity-ani)\n- [Developer notes](#developer-notes)\n - [Code Style and Pre-Commit Hooks](#code-style-and-pre-commit-hooks)\n- [Licensing](#licensing)\n\n\n\n## Overview\n`pyani` is a Python3 module that provides support for calculating average nucleotide identity (ANI) and related measures for whole genome comparisons, and rendering relevant graphical summary output. Where available, it takes advantage of multicore systems, and can integrate with [SGE/OGE](http://gridscheduler.sourceforge.net/)-type job schedulers for the sequence comparisons.\n\n`pyani` installs the following scripts into the `$PATH`:\n\n* `average_nucleotide_identity.py` that enables command-line ANI analysis.\n* `genbank_get_genomes_by_taxon.py` that downloads publicly-available genomes from NCBI.\n* `delta_filter_wrapper.py` is a helper script required to run delta-filter on SGE/OGE systems.\n\n## Installation\n\nThe easiest way to install `pyani` is to use `pip3`:\n\n```bash\npip3 install pyani\n```\n\nFrom version 0.1.3.2 onwards, this should also install all the required Python package dependencies. Prior to this version (i.e. 0.1.3.1 and earlier), you can acquire these dependencies with `pip -r`, and pointing at `requirements.txt` from this repository:\n\n```bash\npip3 install -r requirements.txt\n```\n\n## Docker images\n\n`pyani`'s scripts are also provided as [Docker](https://www.docker.com/) images, that can be run locally as containers. To use these images, first install Docker, then to run the corresponding scripts issue either:\n\n```bash\ndocker run -v ${PWD}:/host_dir leightonpritchard/average_nucleotide_identity\n```\n\nor\n\n```bash\ndocker run -v ${PWD}:/host_dir leightonpritchard/genbank_get_genomes_by_taxon\n```\n\nThe `-v ${PWD}:/host_dir` argument enables the Docker container to see the current directory. Without this argument, the container will not be able to see your input files, or write output data.\n\n\n## Testing `pyani`\n\n`pyani` includes tests that can be run with `nosetest` (including coverage measurement using `coverage.py`) with the following command, executed from the repository root directory:\n\n```bash\nnosetests --cover-erase --cover-package=pyani --cover-html --with-coverage\n```\n\nCoverage output will be placed (by default) in the `cover` subdirectory, and can be loaded into the web browser.\n\n## Running `pyani`\n\n### Script: `average_nucleotide_identity.py`\n\nThe `average_nucleotide_identity.py` script - installed as part of this package - enables straightforward ANI analysis at the command-line, and uses the `pyani` module behind the scenes.\n\nYou can get a summary of available command-line options with `average_nucleotide_identity.py -h`\n\n```bash\n$ average_nucleotide_identity.py -h\nusage: average_nucleotide_identity.py [-h] [-o OUTDIRNAME] [-i INDIRNAME] [-v]\n [-f] [-s FRAGSIZE] [-l LOGFILE]\n [--skip_nucmer] [--skip_blastn]\n [--noclobber] [--nocompress] [-g]\n [--gformat GFORMAT] [--gmethod GMETHOD]\n [--labels LABELS] [--classes CLASSES]\n [-m METHOD] [--scheduler SCHEDULER]\n [--workers WORKERS]\n [--SGEgroupsize SGEGROUPSIZE]\n [--maxmatch] [--nucmer_exe NUCMER_EXE]\n [--blastn_exe BLASTN_EXE]\n [--makeblastdb_exe MAKEBLASTDB_EXE]\n [--blastall_exe BLASTALL_EXE]\n [--formatdb_exe FORMATDB_EXE]\n [--write_excel] [--subsample SUBSAMPLE]\n [--seed SEED] [--jobprefix JOBPREFIX]\n\n\n[\u2026]\n```\n\nExample data and output can be found in the directory `test_ani_data`. The data are chromosomes of four isolates of *Caulobacter*. Basic analyses can be performed with the command lines:\n\n```bash\n$ average_nucleotide_identity.py -i tests/test_ani_data/ -o tests/test_ANIm_output -m ANIm -g\n$ average_nucleotide_identity.py -i tests/test_ani_data/ -o tests/test_ANIb_output -m ANIb -g\n$ average_nucleotide_identity.py -i tests/test_ani_data/ -o tests/test_ANIblastall_output -m ANIblastall -g\n$ average_nucleotide_identity.py -i tests/test_ani_data/ -o tests/test_TETRA_output -m TETRA -g\n```\n\nThe graphical output below, supporting assignment of `NC_002696` and `NC_011916` to the same species (*C.crescentus*), and the other two isolates to distinct species (`NC_014100`:*C.segnis*; `NC_010338`:*C.* sp K31), was generated with the command-line:\n\n```bash\naverage_nucleotide_identity.py -v -i tests/test_ani_data/ \\\n -o tests/test_ANIm_output/ -g --gformat png,pdf,eps \\\n --classes tests/test_ani_data/classes.tab \\\n --labels tests/test_ani_data/labels.tab\n```\n\n\n![ANIm percentage identity for *Caulobacter* test data](tests/test_ani_data/ANIm_percentage_identity.png \"ANIm percentage identity\")\n![ANIm alignment coverage for *Caulobacter* test data](tests/test_ani_data/ANIm_alignment_coverage.png \"ANIm alignment coverage\")\n![ANIm alignment length for *Caulobacter* test data](tests/test_ani_data/ANIm_alignment_lengths.png \"ANIm alignment length\")\n![ANIm alignment similarity errors for *Caulobacter* test data](tests/test_ani_data/ANIm_similarity_errors.png \"ANIm alignment similarity\")\n\n### Script: `genbank_get_genomes_by_taxon.py`\n\nThe script `genbank_get_genomes_by_taxon.py`, installed by this package, enables download of genomes from NCBI, specified by taxon ID. The script will download all available assemblies for taxa at or below the specified node in the NCBI taxonomy tree.\n\nCommand-line options can be viewed using:\n\n```bash\n$ genbank_get_genomes_by_taxon.py -h\nusage: genbacnk_get_genomes_by_taxon.py [-h] [-o OUTDIRNAME] [-t TAXON] [-v]\n [-f] [--noclobber] [-l LOGFILE]\n [--format FORMAT] [--email EMAIL]\n [--retries RETRIES]\n [--batchsize BATCHSIZE]\n[\u2026]\n```\n\nFor example, the NCBI taxonomy ID for *Caulobacter* is 75, so all publicly-available *Caulobacter* sequences can be obtained using the command-line:\n\n```bash\n$ genbank_get_genomes_by_taxon.py -o Caulobacter_downloads -v -t 75 -l Caulobacter_downloads.log --email me@my.email.domain\nINFO: genbank_get_genomes_by_taxon.py: Mon Apr 18 17:22:54 2016\nINFO: command-line: /Users/lpritc/Virtualenvs/pyani3/bin/genbank_get_genomes_by_taxon.py -o Caulobacter_downloads -v -t 75 -l Caulobacter_downloads.log --email me@my.email.domain\nINFO: Namespace(batchsize=10000, email='me@my.email.domain', force=False, format='gbk,fasta', logfile='Caulobacter_downloads.log', noclobber=False, outdirname='Caulobacter_downloads', retries=20, taxon='75', verbose=True)\nINFO: Set NCBI contact email to me@my.email.domain\nINFO: Creating directory Caulobacter_downloads\nINFO: Output directory: Caulobacter_downloads\nINFO: Passed taxon IDs: 75\nINFO: Entrez ESearch with query: txid75[Organism:exp]\nINFO: Entrez ESearch returns 29 assembly IDs\nINFO: Identified 29 unique assemblies\nINFO: Taxon 75: 29 assemblies\n[\u2026]\nINFO: Assembly 639581: 271 contigs\nINFO: Assembly 233261: 17 contigs\nINFO: Assembly 575291: 48 contigs\nINFO: Mon Apr 18 17:25:46 2016\nINFO: Done.\n```\n\n**NOTE:** You must provide a valid email to identify yourself to NCBI for troubleshooting.\n\nThe number of attempted retries for each download, and the size of a batch download can be modified. By default, the script will attempt 20 download retries, and obtain sequences in batches of 10000.\n\n\n## DEPENDENCIES\n\nNote that Python package dependencies should automatically be installed if you are using version 0.1.3.2 or greater, and installing with `pip install pyani`.\n\nFor earlier versions, you can satisfy dependencies by using `pip install -r requirements.txt` (using the `requirements.txt` file in this repository).\n\n### For ANI analysis\n\n* **Biopython** \n* **NumPy** \n* **pandas** \n* **SciPy** \n\n#### Alignment tools\n\n* **BLAST+** executable in the `$PATH`, or available on the command line (required for **ANIb** analysis) \n* **legacy BLAST** executable in the `$PATH` or available on the command line (required for **ANIblastall** analysis) \n* **MUMmer** executables in the $PATH, or available on the command line (required for **ANIm** analysis) \n\n### For graphical output\n\n* **matplotlib** \n* **seaborn** \n\n## Method and Output Description\n\n### Average Nucleotide Identity (ANI)\n\nThis module calculates Average Nucleotide Identity (ANI) according to one of a number of alternative methods described in, e.g.\n\n* Richter M, Rossello-Mora R (2009) Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 106: 19126-19131. doi:10.1073/pnas.0906412106. (ANI1020, ANIm, ANIb)\n* Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P, et al. (2007) DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Micr 57: 81-91. doi:10.1099/ijs.0.64483-0.\n\nANI is proposed to be the appropriate *in silico* substitute for DNA-DNA \nhybridisation (DDH), and so useful for delineating species boundaries. A \ntypical percentage threshold for species boundary in the literature is 95% \nANI (e.g. Richter et al. 2009).\n\nAll ANI methods follow the basic algorithm:\n\n- Align the genome of organism 1 against that of organism 2, and identify the matching regions\n- Calculate the percentage nucleotide identity of the matching regions, as an average for all matching regions\n\nMethods differ on: (1) what alignment algorithm is used, and the choice of parameters (this affects the aligned region boundaries); (2) what the input is for alignment (typically either fragments of fixed size, or the most complete assembly available).\n\n* **ANIm**: uses MUMmer (NUCmer) to align the input sequences.\n* **ANIb**: uses BLASTN+ to align 1020nt fragments of the input sequences\n* **ANIblastall**: uses legacy BLASTN to align 1020nt fragments of the input sequences\n* **TETRA**: calculates tetranucleotide frequencies of each input sequence\n\nThe algorithms takes as input correctly-formatted FASTA multiple sequence files. All sequences for a single organism should be contained in only one sequence file. Although it is possible to provide new labels for each input genome, for rendering graphical output, the names of these files are used for identification so it is best to name \nthem sensibly.\n\nOutput is written to a named directory. The output files differ depending on the chosen ANI method.\n\n* **ANIm**: MUMmer/NUCmer .delta files, describing each pairwise sequence alignment. Output as tab-separated plain text format tables describing: alignment coverage; total alignment lengths; similarity errors; and percentage identity (ANIm).\n* **ANIb** and **ANIblastall**: FASTA sequences describing 1020nt fragments of each input sequence; BLAST nucleotide databases - one for each set of fragments; and BLASTN output files (tab-separated tabular format plain text) - one for each pairwise comparison of input sequences. Output as tab-separated plain text tables describing: alignment coverage; total alignment lengths; similarity errors; and percentage identity (ANIb or ANIblastall).\n* **TETRA**: Tab-separated plain text files describing the Pearson correlations between Z-score distributions for each tetranucleotide in each input sequence (TETRA).\n\nIf graphical output is chosen, the output directory will also contain PDF, PNG and EPS files representing the various output measures as a heatmap with row and column dendrograms. Other output formats (e.g. SVG) can be specified with the `--gformat` argument.\n\n## Developer notes\n\nThe `pyani` package is presented at [`GitHub`](https://github.com/widdowquinn/pyani) under two main branches:\n\n- `master` is the source code underpinning the most recent/current release of `pyani`. It will (almost) always be in sync with the latest release found at [https://github.com/widdowquinn/pyani/releases](https://github.com/widdowquinn/pyani/releases). The only time this code should not be in sync with the release is when there are modifications to documentation, or immediately preceding a release.\n- `development` is the current bleeding-edge version of `pyani`. It should (almost) always be in a working and usable condition, but may not be complete and/or some features may be missing or still under development.\n\n###\u00a0Code Style and Pre-Commit Hooks\n\nThe source code for `pyani` is expected to conform to `flake8` linting, and `black` code styling. These are enforced as pre-commit hooks using the `pre-commit` package (included in `requirements.txt`).\n\nThe `black` and `flake8` hooks are defined in `.pre-commit-config.yaml`. Custom settings for `flake8` are held in `.flake8`.\n\nTo enable pre-commit checks in the codebase on your local machine, execute the following command in the root directory of this repository:\n\n```bash\npre-commit install\n```\n\n## Licensing\n\nUnless otherwise indicated, all code is subject to the following agreement:\n\n (c) The James Hutton Institute 2014-2019\n Author: Leighton Pritchard\n\n Contact: leighton.pritchard@hutton.ac.uk\n\n Address: \n Leighton Pritchard,\n Information and Computational Sciences,\n James Hutton Institute,\n Errol Road,\n Invergowrie,\n Dundee,\n DD6 9LH,\n Scotland,\n UK\n\nThe MIT License\n\nCopyright (c) 2014-2019 The James Hutton Institute\n\nPermission is hereby granted, free of charge, to any person obtaining a copy\nof this software and associated documentation files (the \"Software\"), to deal\nin the Software without restriction, including without limitation the rights\nto use, copy, modify, merge, publish, distribute, sublicense, and/or sell\ncopies of the Software, and to permit persons to whom the Software is\nfurnished to do so, subject to the following conditions:\n\nThe above copyright notice and this permission notice shall be included in\nall copies or substantial portions of the Software.\n\nTHE SOFTWARE IS PROVIDED \"AS IS\", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR\nIMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,\nFITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE\nAUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER\nLIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM,\nOUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN\nTHE SOFTWARE.\n\n\n",
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