A bacterial transcriptome annotation pipeline based on RNA-Seq
Project description
About ANNOgesic
ANNOgesic is a modular, command-line tool that can integrate different types of RNA-Seq data like dRNA-Seq or RNA-Seq generated after transcript fragmentation and generates high quality genome annotations. It can detect genes, CDSs/tRNAs/rRNAs, transcription starting sites (TSS) and processing sites, transcripts, terminators, untranslated regions (UTR) as well as small RNAs (sRNA), small open reading frames (sORF), circular RNAs, CRISPR related RNAs, riboswitches and RNA-thermometers. It can also perform RNA-RNA and protein-protein interactions prediction. Furthermore, it groups genes into operons and sub-operons and reveal promoter motifs. It can also allocate GO term and subcellular localization to genes. Several of ANNOgesic features are new implementation while others are performed and improved by third-party tools and for some of them adaptive parameter-optimizations were included. Additionally, numerous visualization and statistics help the user quickly evaluated feature predictions resulting from an ANNOgesic analysis. The pipeline is modular and was heavily tested with several RNA-Seq data set from bacterial as well as archaeal samples.
Documentation
Documentation can be found on here.
Installation
Short version (if you have all the requirements installed):
$ pip3 install ANNOgesic
If you want to know the requirement, please refer to Documentation.
Arguments
usage: annogesic [-h] [--version] {create,get_input_files,update_genome_fasta, annotation_transfer,tss_ps,optimize_tss_ps, terminator,transcript,utr,srna,sorf,promoter,operon, circrna,go_term,srna_target,snp,ppi_network, localization,riboswitch_thermometer,crispr, merge_features,screenshot,color_png} ... positional arguments: {create,get_input_files,update_genome_fasta,annotation_transfer,tss_ps, optimize_tss_ps,terminator,transcript,utr,srna,sorf,promoter,operon, circrna,go_term,srna_target,snp,ppi_network,localization, riboswitch_thermometer,crispr,merge_features,screenshot,color_png} commands create Create a project get_input_files Get required files. (i.e. Annotation files, fasta files) update_genome_fasta Get fasta files of query genomes if the query sequences do not exist. annotation_transfer Transfer the annotations from closed genome to the target genome. tss_ps Detect TSSs or processing sites. optimize_tss_ps Optimize TSSs or processing sites based on manual detected ones. terminator Detect rho-independent terminators. transcript Detect transcripts based on coverage file. utr Detect 5'UTRs and 3'UTRs. srna Detect intergenic, antisense and UTR-derived sRNAs. sorf Detect expressed sORFs. promoter Discover promoter motifs. operon Detect operons and sub-operons. circrna Detect circular RNAs. go_term Extract Go terms from Uniprot. srna_target Detect sRNA-mRNA interactions. snp Detect SNP/mutation and generate potential fasta file. ppi_network Detect protein-protein interactions with literature supported. localization Predict subcellular localization of CDSs. riboswitch_thermometer Predict riboswitches and RNA thermometers. crispr Predict CRISPR related RNAs. merge_features Merge all features to one gff file. screenshot Generate screenshot for selected feature. color_png Generate color screenshots of TSS or processing site. It only works after running "screenshot" (after running batch script). optional arguments: -h, --help show this help message and exit --version, -v show version
License
ISC (Internet Systems Consortium license ~ simplified BSD license) - see LICENSE
Contact
If you have any questions, please contact Sung-Huan Yu
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