There is no official publication for MagicLamp. If it was useful for your work, please cite as follows:
Garber, AI., Ramirez, GA., Merino, N., Pavia MJ., McAllister, SM. (2020) MagicLamp: toolkit for annotation of 'omics datasets using curated HMM sets. 2021: MagicLamp, GitHub repository: https://github.com/Arkadiy-Garber/MagicLamp.
git clone https://github.com/Arkadiy-Garber/MagicLamp.git
cd MagicLamp
bash setup.sh
source activate magiclamp
(if "source activate magiclamp" does not work, you can use "conda activate magiclamp")
Put MagicLamp.py script $PATH into your bash profile
export PATH=$PATH:$(pwd)
- Python (version 3.6 or higher)
- BLAST (version 2.7.1+)
- Prodigal (version 2.6.3)
- HMMER (version 3.2.1)
- Diamond (version 0.9.22.123) -- if you performing cross-validation against a reference database
- R (version 3.5.1) -- if generating plots
- Rscript -- if generating plots
There are two tutorials available for this software, available in this repository's wiki: https://github.com/Arkadiy-Garber/MagicLamp/wiki#welcome-to-the-magiclamp-wiki
An improtant feature of MagicLamp is the ability of users to use their own HMM sets with HmmGenie, like so:
MagicLamp.py HmmGenie -bin_dir bins/ -bin_ext fna -hmm_dir HMMs/ -hmm_ext hmm -rules rules-template.csv
In the above example, the HMMs/ directory contains the user-compiled or created HMMs, where each HMM file ends with a .hmm filename extension. The rules-template.csv file is provided in the main MagicLamp repository (should be in the same folder as this readme). Users are to fill out this file, providing information on each HMM that they wish to use with this program.
We encourage users to submit their custom-built or compiled HMM sets for specific pathways or processes. Please email the following material to agarber4@asu.edu: 1) zipped folder containing the HMM files, 2) filled-out rules-template.csv file. Optionally, users can also provide 1) genome(s) known to encode the genetic pathway(s), and 2) genome(s) known not to encode the genetic pathway.
(for a list of all available genies)
MagicLamp.py help
(for a detailed help menu for each genie)
MagicLamp.py FeGenie -h
MagicLamp.py LithoGenie -h
MagicLamp.py WspGenie -h
MagicLamp.py GasGenie -h
MagicLamp.py MagnetoGenie -h
MagicLamp.py RosGenie -h
MagicLamp.py Lucifer -h
MagicLamp.py HmmGenie -h
MagicLamp.py FeGenie -bin_dir genomes/ -bin_ext fna -out fegenie_output
MagicLamp.py FeGenie -bin_dir genomes/ -bin_ext fna -out fegenie_output --orfs
MagicLamp.py FeGenie -bin_dir genomes/ -bin_ext fna -out fegenie_output --gbk
if you want to normalize the number of identified genes to the total number of ORFs in the dataset, use the --norm flag
MagicLamp.py FeGenie -bin_dir genomes/ -bin_ext fna -out fegenie_output --norm
MagicLamp.py LithoGenie -bin_dir genomes/ -bin_ext fna -out lithogenie_output -cat sulfur
if you already ran LithoGenie once, but want to re-do the heatmap file with a different category, use the --skip flag
MagicLamp.py LithoGenie -bin_dir genomes/ -bin_ext fna -out lithogenie_output --cat iron --skip
you can also include prediction of signal peptides and transmembrane domains with Phobius, using the --phobius flag
MagicLamp.py LithoGenie -bin_dir genomes/ -bin_ext fna -out lithogenie_output --cat iron --skip
full list of LithoGenie categories (default action of the program is to create a broad-category heatmap)
- iron
- sulfur
- nitrogen
- oxygen
- methane
- hydrogen
- arsenic
- nitriles
- manganese
- carbon-monoxide
- halogenetated-compounds
- C1compounds
- urea
- selenium
many of the HMMs used by LithoGenie were developed and compiled by Karthik Anantharaman: https://github.com/kanantharaman/metabolic-hmms
Phobius is not available through Anaconda, so the executables (phobius.pl, phobius.options, phobius.model, decodeanhmm, and decodeanhmm.64bit) are included in this repository. Standalone copy of Phobius was obtained from the following website: https://phobius.sbc.su.se/data.html, and users should cite the following article:
Käll, L., Krogh, A., & Sonnhammer, E. L. L. (2004). A combined transmembrane topology and signal peptide prediction method. Journal of Molecular Biology, 338(5), 1027–1036.