[![Build Status](https://travis-ci.org/tseemann/barrnap.svg?branch=master)](https://travis-ci.org/tseemann/barrnap) [![License: GPL v3](https://img.shields.io/badge/License-GPL%20v3-blue.svg)](https://www.gnu.org/licenses/gpl-3.0) [](#lang-au) # Barrnap BAsic Rapid Ribosomal RNA Predictor ## Description Barrnap predicts the location of ribosomal RNA genes in genomes. It supports bacteria (5S,23S,16S), archaea (5S,5.8S,23S,16S), metazoan mitochondria (12S,16S) and eukaryotes (5S,5.8S,28S,18S). It takes FASTA DNA sequence as input, and write GFF3 as output. It uses the new `nhmmer` tool that comes with HMMER 3.1 for HMM searching in RNA:DNA style. Multithreading is supported and one can expect roughly linear speed-ups with more CPUs. ## Installation ### Requirements * [Perl 5.xx](https://dev.perl.org/perl5/) (core modules only) * [nhmmer](https://hmmer.org/) (part of HMMER 3.x) * [bedtools](http://bedtools.readthedocs.io/en/latest/) ### Conda Install [Conda](https://conda.io/docs/) or [Miniconda](https://conda.io/miniconda.html): ``` conda -c bioconda -c conda-forge install barrnap barrnap --version ``` ### Homebrew Install [HomeBrew](http://brew.sh/) (Mac OS X) or [LinuxBrew](http://brew.sh/linuxbrew/) (Linux). ``` brew install brewsci/bio/barrnap barrnap --help ``` ### Source This will install the latest version direct from Github. You'll need to add the `bin` directory to your PATH. ``` cd $HOME tar zxvf barrnap-0.X.tar.gz barrnap-0.X/barrnap -h ``` ## Usage ``` % barrnap --quiet examples/small.fna ##gff-version 3 P.marinus barrnap:0.8 rRNA 353314 354793 0 + . Name=16S_rRNA;product=16S ribosomal RNA P.marinus barrnap:0.8 rRNA 355464 358334 0 + . Name=23S_rRNA;product=23S ribosomal RNA P.marinus barrnap:0.8 rRNA 358433 358536 7.5e-07 + . Name=5S_rRNA;product=5S ribosomal RNA % barrnap -q -k mito examples/mitochondria.fna ##gff-version 3 AF346967.1 barrnap:0.8 rRNA 643 1610 . + . Name=12S_rRNA;product=12S ribosomal RNA AF346967.1 barrnap:0.8 rRNA 1672 3228 . + . Name=16S_rRNA;product=16S ribosomal RNA % barrnap -o rrna.fa < contigs.fa > rrna.gff % head -n 3 rrna.fa >16S_rRNA::gi|329138943|tpg|BK006945.2|:455935-456864(-) ACGGTCGGGGGCATCAGTATTCAATTGTCAGAGGTGAAATTCTTGGATT TATTGAAGACTAACTACTGCGAAAGCATTTGCCAAGGACGTTTTCATTA ``` ## Options ### General * `--help` show help and exit * `--version` print version in form `barrnap X.Y` and exit * `--citation` print a citation and exit ### Search * `--kingdom` is the database to use: Bacteria:`bac`, Archaea:`arc`, Eukaryota:`euk`, Metazoan Mitochondria:`mito` * `--threads` is how many CPUs to assign to `nhmmer` search * `--evalue` is the cut-off for `nhmmer` reporting, before further scrutiny * `--lencutoff` is the proportion of the full length that qualifies as `partial` match * `--reject` will not include hits below this proportion of the expected length ### Output * `--quiet` will not print any messages to `stderr` * `--incseq` will include the full input sequences in the output GFF * `--outseq` creates a FASTA file with the hit sequences ## Caveats Barrnap does not do anything fancy. It has HMM models for each different rRNA gene. They are built from full length seed alignments. ## Comparison with RNAmmer Barrnap is designed to be a substitute for [RNAmmer](http://www.cbs.dtu.dk/services/RNAmmer/). It was motivated by my desire to remove [Prokka's](https://github.com/tseemann/prokka) dependency on RNAmmer which is encumbered by a free-for-academic sign-up license, and by RNAmmer's dependence on legacy HMMER 2.x which conflicts with HMMER 3.x that most people are using now. RNAmmer is more sophisticated than Barrnap, and more accurate because it uses HMMER 2.x in glocal alignment mode whereas NHMMER 3.x currently only supports local alignment (Sean Eddy expected glocal to be supported in 2014, but it still isn't available in 2018). In practice, Barrnap will find all the typical rRNA genes in a few seconds (in bacteria), but may get the end points out by a few bases and will probably miss wierd rRNAs. The HMM models it uses are derived from Rfam, Silva and RefSeq. ## Data sources for HMM models ``` Bacteria (70S) LSU 50S 5S RF00001 23S SILVA-LSU-Bac SSU 30S 16S RF00177 Archaea (70S) LSU 50S 5S RF00001 5.8S RF00002 23S SILVA-LSU-Arc SSU 30S 16S RF01959 Eukarya (80S) LSU 60S 5S RF00001 5.8S RF00002 28S SILVA-LSU-Euk SSU 40S 18S RF01960 Metazoan Mito 12S RefSeq (MT-RNR1, s-rRNA, rns) 16S RefSeq (MT-RNR2, l-rRNA, rnl) ``` ## Models I would like to add ``` Fungi [Sajeet Haridas] LSU 35S ? 5S 5.8S 25S SSU ? 18S Mito [http://www.ncbi.nlm.nih.gov/nuccore/NC_001224.1] 15S 21S (multiple exons) Apicoplast [http://www.ncbi.nlm.nih.gov/nuccore/U87145.2] LSU ~2500bp 28S ? SSU ~1500bp 16S ? Plant [Shaun Jackman] Mito [https://www.ncbi.nlm.nih.gov/nucleotide?cmd=Retrieve&dopt=GenBank&list_uids=26556996] 5S ~118 bp ? rrn5 (use RF00001 ?) 18S ~1935 bp ? rrn18 (use RF01960 ?) 26S ~2568 bp ? rrn26 ``` ## Where does the name come from? The name Barrnap was originally derived from _Bacterial/Archaeal Ribosomal RNA Predictor_. However it has since been extended to support mitochondrial and eukaryotic rRNAs, and has been given the new backronym _BAsic Rapid Ribosomal RNA Predictor_. The project was originally spawned at CodeFest 2013 in Berlin, Germany by Torsten Seemann and Tim Booth. ## License * Barrnap: [GPLv3](https://raw.githubusercontent.com/tseemann/barrnap/master/LICENSE) * Rfam: [CC0](https://raw.githubusercontent.com/tseemann/barrnap/master/LICENSE.Rfam) * SILVA: [Free for academic use](https://raw.githubusercontent.com/tseemann/barrnap/master/LICENSE.SILVA) ## Author Torsten Seemann