Skip to content

A Fully Automatic Method for Predicting Contact Maps of RNAs by Evolutionary Coupling Analysis

Notifications You must be signed in to change notification settings

jaswindersingh2/RNAcmap

Repository files navigation

RNAcmap

A Fully Automatic Method for Predicting Contact Maps of RNAs by Evolutionary Coupling Analysis

SYSTEM REQUIREMENTS

Hardware Requirments:

RNAcmap predictor requires only a standard computer with around 32 GB RAM to support the in-memory operations for RNAs sequence length less than 500.

Software Requirments:

RNAcmap has been tested on Ubuntu 14.04, 16.04, and 18.04 operating systems.

USAGE

Installation:

To install RNAcmap and it's dependencies following commands can be used in terminal:

  1. git clone https://github.com/jaswindersingh2/RNAcmap.git
  2. cd RNAcmap

Either follow virtualenv column steps or conda column steps to create virtual environment and to install RNAcmap python dependencies given in table below:

                      virtualenv                                      conda
3. virtualenv -p python3.6 venv_rnacmap conda create -n venv_rnacmap python=3.6
4. source ./venv_rnacmap/bin/activate conda activate venv_rnacmap
5. pip install -r requirements.txt && deactivate while read p; do conda install --yes $p; done < requirements.txt && conda deactivate

If Infernal tool is alread installed in the system, please add path to binary files in line no. 9 of 'run_rnacmap.sh' file. In case, Infernal tool is not installed in the system, please use follwing 2 command to download and extract it. In case of any problem and issue regarding Infernal download, please refer to Infernal webpage as following commands only tested on Ubuntu 18.04, 64 bit system.

  1. wget 'eddylab.org/infernal/infernal-1.1.3-linux-intel-gcc.tar.gz'
  2. tar -xvzf infernal-*.tar.gz && rm infernal-*.tar.gz

If BLASTN tool is alread installed in the system, please add path to binary files in line no. 7 of 'run_rnacmap.sh' file. In case, BLASTN tool is not installed in the system, please use follwing 2 command to download and extract it. In case of any problem and issue regarding BLASTN download, please refer to BLASTN webpage as following commands only tested on Ubuntu 18.04, 64 bit system.

  1. wget 'ftp://ftp.ncbi.nlm.nih.gov/blast/executables/blast+/LATEST/ncbi-blast-*+-x64-linux.tar.gz'
  2. tar -xvzf ncbi-blast-*+-x64-linux.tar.gz && rm ncbi-blast-*+-x64-linux.tar.gz

Either install RNAfold or SPOT-RNA predictor depending upon which Secondary Structure predictor you want to use. Installation of RNAfold will take 15-20 mins and 2-3 mins for SPOT-RNA. Both the secondary structure can be installed as well if you want to predict for both predictors. In case of issue regarding installation of these predictors, please refer to more specific and detailed guide for ViennaRNA and SPOT-RNA.

  1. ./install_RNAfold.sh or/and ./install_SPOT-RNA.sh

If NCBI's nt database already available in your system, please add path to database in line no. 8 and line 10 of 'run_rnacmap.sh' file. Otherwise, download the reference database (NCBI's nt database) for BLASTN and INFERNAL. The following command can used for NCBI's nt database. Make sure there is enough space on the system as NCBI's nt database is of size around 270 GB after extraction and it can take couple of hours to download depending on the internet speed. In case of any issue, please rerfer to NCBI's database website.

  1. wget -c "ftp://ftp.ncbi.nlm.nih.gov/blast/db/FASTA/nt.gz" -O ./nt_database/nt.gz && gunzip ./nt_database/nt.gz

This NCBI's database need to formated to use with BLASTN tool. To format the NCBI's database, the following command can be used. Please make sure system have enough space as formated database is of size around 120 GB in addition to appox. 270 GB from previous step and it can few hours for it.

  1. ./ncbi-blast-2.10.0+/bin/makeblastdb -in ./nt_database/nt -dbtype nucl

To install the DCA predictor, please run the following command:

  1. ./install_GREMLIN.sh or/and ./install_plmc.sh

To run the RNAcmap

To run the RNAcmap, the following command can be used. Use either RNAfold or SPOT-RNA for secondary structure predictor and one DCA method among GREMLIN, plmc, and mfDCA as input argument.

./run_rnacmap.sh inputs/sample_seq.fasta RNAfold/SPOT-RNA GREMLIN/plmc/mfDCA

The final output will be the "*.dca" file in the "outputs" folder consists of predicted Direct Coupling Analysis (DCA) by RNAcmap for a given input RNA sequence.

References

If you use RNAcmap for your research please cite the following papers:

Zhang, T., Singh, J., Litfin, T., Zhan, J., Paliwal, K. and Zhou, Y., 2021. RNAcmap: a fully automatic pipeline for predicting contact maps of RNAs by evolutionary coupling analysis. Bioinformatics, 37(20), pp.3494-3500.

Other references:

[1] Nawrocki, E.P. and Eddy, S.R., 2013. Infernal 1.1: 100-fold faster RNA homology searches. Bioinformatics, 29(22), pp.2933-2935..

[2] Hofacker, I.L., 2003. Vienna RNA secondary structure server. Nucleic acids research, 31(13), pp.3429-3431.

[3] H.M. Berman, J. Westbrook, Z. Feng, G. Gilliland, T.N. Bhat, H. Weissig, I.N. Shindyalov, P.E. Bourne. (2000) The Protein Data Bank Nucleic Acids Research, 28: 235-242.

[4] Singh, J., Hanson, J., Paliwal, K. and Zhou, Y., 2019. RNA secondary structure prediction using an ensemble of two-dimensional deep neural networks and transfer learning. Nature communications, 10(1), pp.1-13.

[5] Kamisetty, H., Ovchinnikov, S. and Baker, D., 2013. Assessing the utility of coevolution-based residue–residue contact predictions in a sequence-and structure-rich era. Proceedings of the National Academy of Sciences, 110(39), pp.15674-15679.

Licence

Mozilla Public License 2.0

Contact

jaswinder.singh3@griffithuni.edu.au, tongchuan.zhang@griffithuni.edu.au, yaoqi.zhou@griffith.edu.au