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PlncPRO (Plant Long Non-Coding rna Prediction by Random fOrests) is a program to classify coding (mRNAs) and long non-coding transcripts (lncRNAs). Our method is based on random forest method and uses protein homology search, sequence based and 3-mer frequency based features. We have developed predictive models for several plant species to predict lncRNAs. We comprehensively tested our method on plants and vertebrates and found that our model works better as compared to the existing tools.
Singh et. al. PLncPRO for prediction of long non-coding RNAs (lncRNAs) in plants and its application for discovery of abiotic stress-responsive lncRNAs in rice and chickpea. Nucleic Acids Res. 2017 Dec 15;45(22):e183. doi: 10.1093/nar/gkx866.
NOTE: We have updated PlncPRO for python3. PlncPRO for python2 is also available at http://ccbb.jnu.ac.in/plncpro/. Usage for this newer version is different from the older versions.
- OS: Linux, macOS
- Python 3.6 or later versions (http://www.python.org/)
- NCBI BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi)
- GNU C Library (glibc >= 2.14)
- NumPy (http://www.numpy.org/)
- SciPy (https://www.scipy.org/)
- Scikit-learn (http://scikit-learn.org/)
- Biopython (http://biopython.org/)
- regex
conda install -c bioconda plncpro
pip install plncpro
git clone https://github.com/urmi-21/PLncPRO.git
pip install PlncPro
bash tests/local_test.sh
See examples for detailed usage examples.
Label lncRNAs and mRNAs. This file reads an input file containing sequences and then classifies the sequences as coding or non-coding. It uses a model generated by build.py to make classifications. It outputs a file containing class label and class probabilities for each sequence.
plncpro predict -i <input fasta> -o <output_dir> -p <output_file_name> -t 2 -d <blast_db> -m <model_file>
-p,--prediction_out output file name
-i,--infile file containing input sequences
-m,--model model file
-o,--outdir output directory name
-d,--db path to blast database
OPTIONAL
-t,--threads number of threads [default: 4]
-l,--labels path to the files containg labels(it outputs classification accuracy)
-r,--remove_temp clean up intermediate files
-v,--verbose show more messages
--min_len specifiy min_length to filter input files
--noblast Don't use blast features
-no_ff Don't use framefinder features
--qcov_hsp specify query coverage parameter for blast[default:30]
--blastres* path to blast output for input file
*blast result should be in following format: -outfmt '6 qseqid sseqid pident evalue qcovs qcovhsp score bitscore qframe sframe'
Build model using the given training data (mRNA/lncRNA transcripts). This file reads two labelled datasets containing coding and non-coding transcripts. Then it makes a random forest based classification model and saves the model, which can be used to predict unknown sequences.
plncpro build -p <mrna fasta> -n <lncrna fasta> -o <out_dir> -m <model_name> -d <blast db> -t <threads>
-p,--pos file containing mRNA sequences
-n,--neg file containing lncRNA sequences
-m,--model output model name
-o,--outdir output directory name
-d path to blast database
OPTIONAL
-t,--threads number of threads [default: 4]
-k,--num_trees number of trees[default: 1000]
-r,--remove_temp clean up intermediate files
-v,--verbose show more messages
--min_len specifiy min_length to filter input files
--noblast Don't use blast features
--no_ff Don't use framefinder features
--qcov_hsp specify query cov parameter for blast[default:30]
--pos_blastres* path to blast result for mRNA input file
--neg_blastres* path to blast result for lncRNA input file
*blast result should be in following format: -outfmt '6 qseqid sseqid pident evalue qcovs qcovhsp score bitscore qframe sframe'
Extract mRNA or lncRNA sequences from PLNCPRO output file. This file reads a prediction output file and extracts sequences from a given class. User can specify class and probability cut-off and extract desired transcript sequences.
plncpro predtoseq -f <fasta_file> -o <outputfile> -p <PLNCPRO_prediction_file> -l <required_label>
-f input fasta file name
-o output fasta file name
-p path to file containg predictions by PLNCPRO
OPTIONAL
-l label of the required sequences (0 for lncRNA;1 for mRNA) [default:0]
-s class probability cutoff (extract sequences with probability greater than or equal to s
--min specifiy min_length of sequences[default:0]
--max specifiy min_length of sequences[default:Inf]
Diamond is several folds faster than blastx and could be used instead of blastx. To use diamond with plncpro, first run diamond using following output parameters:
diamond blastx -d <diamondDB> -q <query.fasta> -o <diamond_out> --outfmt 6 qseqid sseqid pident evalue nident qcovhsp score bitscore qframe qstrand
Then pass the diamond output using the --blastres parameter to plncpro, e.g.:
plncpro predict -i <input.fasta> -o <outfile> -p <preds> --blastres <diamond_out> -m <model>
Data is hosted on google drive. Direct link
Directly download using wget.
wget --load-cookies /tmp/cookies.txt "https://docs.google.com/uc?export=download&confirm=$(wget --quiet --save-cookies /tmp/cookies.txt --keep-session-cookies --no-check-certificate 'https://docs.google.com/uc?export=download&id=108S-9Bt4CLCHTaCn6-HKTqQZDo0nssZe' -O- | sed -rn 's/.*confirm=([0-9A-Za-z_]+).*/\1\n/p')&id=108S-9Bt4CLCHTaCn6-HKTqQZDo0nssZe" -O plncpro_data.zip && rm -rf /tmp/cookies.txt
GNU Public License version 3 (GPLv3) Details on http://www.gnu.org/copyleft/gpl.html