4.8 Article

GraftM: a tool for scalable, phylogenetically informed classification of genes within metagenomes

Journal

NUCLEIC ACIDS RESEARCH
Volume 46, Issue 10, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gky174

Keywords

-

Funding

  1. Genomic Science Program of the United States Department of Energy Office of Biological and Environmental Research [DE-SC0004632, DE-SC0010580, DE-SC0016440]
  2. Australian Research Council (ARC)
  3. ARC Discovery Early Career Researcher Award [DE-160100248]
  4. University of Queensland Vice Chancellor Research Focused Fellowship
  5. Australian Research Council [DE-160100248]
  6. U.S. Department of Energy, Office of Science, Biological and Environmental Research [DE-SC0004632]

Ask authors/readers for more resources

Large-scale metagenomic datasets enable the recovery of hundreds of population genomes from environmental samples. However, these genomes do not typically represent the full diversity of complex microbial communities. Gene-centric approaches can be used to gain a comprehensive view of diversity by examining each read independently, but traditional pairwise comparison approaches typically over-classify taxonomy and scale poorly with increasing metagenome and database sizes. Here we introduce GraftM, a tool that uses gene specific packages to rapidly identify gene families in metagenomic data using hidden Markov models (HMMs) or DIAMOND databases, and classifies these sequences using placement into pre-constructed gene trees. The speed and accuracy of GraftM was benchmarked with in silico and in vitro mock communities using taxonomic markers, and was found to have higher accuracy at the family level with a processing time 2.0-3.7x faster than currently available software. Exploration of a wetland metagenome using 16S rRNA-and methyl-coenzyme M reductase (McrA)specific gpkgs revealed taxonomic and functional shifts across a depth gradient. Analysis of the NCBI nr database using the McrA gpkg allowed the detection of novel sequences belonging to phylum-level lineages.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available