MetaPathways

MetaPathways annotates and infers metabolic pathways from metagenomic and metatranscriptomic next-generation sequencing data to characterize ecological and biogeochemical functions of microbial communities.


Key Features:

  • Operational Stages: Processes data through four stages—Quality Control, Feature Prediction, Functional Annotation, and Pathway Inference—to transform raw sequences into functional outputs.
  • Quality Control and Assessment: Performs quality assessment and control on both assembled and unassembled nucleotide sequences from next-generation sequencing datasets.
  • Feature Prediction and Annotation: Predicts and annotates noncoding genes and open reading frames (ORFs) to support downstream functional assignment.
  • Pathway Inference with PathoLogic: Maps functional annotations onto the MetaCyc database using the PathoLogic algorithm to construct environmental Pathway/Genome Databases (ePGDBs), as an alternative to KEGG or SEED-based approaches, and produces ePGDBs compatible with Pathway Tools.
  • Phylogenetic Analysis: Builds phylogenetic trees using MLTreeMap based on selected taxonomic anchor and functional gene markers.
  • Data Conversion and Output Formats: Converts General Feature Format (GFF) files into concatenated GenBank files for ePGDB construction, generates Sequin files for GenBank submission, and produces comprehensive gene feature tables.
  • Quantitative Comparison and Pathway Prediction: Integrates a weighted taxonomic distance metric and a normalized read-mapping measure to improve pathway prediction and enable quantitative comparison of assembled annotations.
  • Improved Homology Searches: Uses LAST with BLAST-equivalent E-values to enhance homology search precision and compatibility with prevailing software.
  • Annotation Mapping to Functional Hierarchies: Supports mapping of annotations onto user-defined functional gene hierarchies, including the Carbohydrate-Active Enzyme (CAZy) database.

Scientific Applications:

  • Metabolic Network Reconstruction: Reconstructs metabolic interaction networks from environmental sequence data to investigate microbial ecological functions.
  • Community Structure and Function Analysis: Generates ePGDBs and MLTreeMap-based phylogenetic trees to analyze microbial community structure, functional potential, and evolutionary relationships across diverse ecosystems.
  • Cross-omic Integration: Applies to metagenomic, metatranscriptomic, genomic, and transcriptomic datasets from various sequencing platforms to explore metabolic pathways and biogeochemical interactions.

Methodology:

Performs quality assessment on assembled and unassembled nucleotide sequences; predicts noncoding genes and ORFs; conducts homology searches with LAST (BLAST-equivalent E-values); maps annotations to MetaCyc via PathoLogic to build ePGDBs; converts GFF to concatenated GenBank and generates Sequin files and gene feature tables; constructs phylogenetic trees with MLTreeMap; and applies weighted taxonomic distance and normalized read-mapping measures for pathway prediction and quantitative comparison.

Topics

Details

License:
MPL-2.0
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux
Programming Languages:
Python
Added:
8/3/2017
Last Updated:
11/24/2024

Operations

Data Inputs & Outputs

Gene functional annotation

Publications

McLaughlin RJ, Liu TX, Altman T, Nallan AN, Hahn AS, Anstett J, Morgan-Lang C, Konwar KM, Hallam SJ. MetaPathways v3.5: Modularity and Scalability Improvements for Pathway Inference from Environmental Genomes. Unknown Journal. 2024. doi:10.1101/2024.06.04.597460.

Konwar KM, Hanson NW, Bhatia MP, Kim D, Wu S, Hahn AS, Morgan-Lang C, Cheung HK, Hallam SJ. MetaPathways v2.5: quantitative functional, taxonomic and usability improvements. Bioinformatics. 2015;31(20):3345-3347. doi:10.1093/bioinformatics/btv361. PMID:26076725. PMCID:PMC4595896.

Konwar KM, Hanson NW, Pagé AP, Hallam SJ. MetaPathways: a modular pipeline for constructing pathway/genome databases from environmental sequence information. BMC Bioinformatics. 2013;14(1). doi:10.1186/1471-2105-14-202. PMID:23800136. PMCID:PMC3695837.

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