lncRNApipe is a pipeline to extract putative novel lncRNAs ab initio, given a list of transcripts in GTF format assembled from deep sequencing data (ex: RNA-Seq) and annotation data. This pipeline script will bind together the functionality of the tools / scripts: cuffcompare, categorize_ncRNAs.pl, get_unique_features.pl, fetch_seq_from_ucsc.pl, RNAfold, Infernal and Coding Potential Calculator (CPC.sh). Transcriptome construction tools such as Cufflinks produces a set of assembled transcripts in GTF format. lncRNApipe uses this data in addition to known gene annotation to extract putative lncRNAs constructed by the ab initio assemblers. The pipeline relies on the FPKM / RPKM values generated by these assemblers to assess the confidence of the constructed de novo transcripts and validates it against the known reference gene and non coding RNA information to identify putative novel lncRNAs. The quality of predicted novel lncRNAs highly depends upon the most up-to-date known gene and / or ncRNA annotation file(s) supplied to the pipeline. IO::Routine The scripts use custom IO::Routine Perl Module. If you are installing lncRNApipe Pipeline, IO::Routine module is automatically installed. Requires Bio::SeqIO module be installed and available. ☲☴ lncRNApipe Head on to NGS-Utils directory for script list. Install lncRNApipe and all its dependencies (Mac and Linux): cd /to/your/preferred/install/path curl -O https://raw.githubusercontent.com/biocoder/Perl-for-Bioinformatics/master/NGS-Utils/lncRNApipe perl lncRNApipe -setup Documentation: perl lncRNApipe -h or perldoc lncRNApipe or to get help documentation for individual modules, do: perl lncRNApipe -h cuff perl lncRNApipe -h cat perl lncRNApipe -h get perl lncRNApipe -h fetch perl lncRNApipe -h cpc perl lncRNApipe -h rna perl lncRNApipe -h inf Known issues: If pipeline setup fails due to XML::Parser module, you need to install XML parser C libraries. On Ubuntu / Debian based Linux distributions, as root user, do: apt-get install libexpat1 libexpat1-dev On RedHat / Fedora / CentOS based Linux distributions, as root user do: yum install expat expat-devel RNAfold: RNAfold is slow and does not work for sequences over 10000bp in length. I am working on including an alternative secondary structure prediction program instead of RNAfold. Meanwhile you may skip running RNAfold module by not issuing the --rnafold option with lncRNApipe. Caveats: The pipeline script uses a lot of inherent Linux core utils and has been only tested in BASH shell. Please use absolute full PATH names. Instead of using lncRNApipe -run ./lncRNApipe_output ..., use lncRNApipe -run /data/lncRNApipe_output ... Citation Konganti, Kranti (2015). lncRNApipe: A pipeline to identify putative novel lncRNAs from deep sequencing data. https://github.com/biocoder/Perl-for-Bioinformatics/releases Cheers, BioCoder