PT - JOURNAL ARTICLE AU - Shea N. Gardner AU - Sasha K. Ames AU - Maya B. Gokhale AU - Tom R. Slezak AU - Jonathan E. Allen TI - Searching more genomic sequence with less memory for fast and accurate metagenomic profiling AID - 10.1101/036681 DP - 2016 Jan 01 TA - bioRxiv PG - 036681 4099 - http://biorxiv.org/content/early/2016/01/14/036681.short 4100 - http://biorxiv.org/content/early/2016/01/14/036681.full AB - Software for rapid, accurate, and comprehensive microbial profiling of metagenomic sequence data on a desktop will play an important role in large scale clinical use of metagenomic data. Here we describe LMAT-ML (Livermore Metagenomics Analysis Toolkit-Marker Library) which can be run with 24 GB of DRAM memory, an amount available on many clusters, or with 16 GB DRAM plus a 24 GB low cost commodity flash drive (NVRAM), a cost effective alternative for desktop or laptop users. We compared results from LMAT with five other rapid, low-memory tools for metagenome analysis for 131 Human Microbiome Project samples, and assessed discordant calls with BLAST. All the tools except LMAT-ML reported overly specific or incorrect species and strain resolution of reads that were in fact much more widely conserved across species, genera, and even families. Several of the tools misclassified reads from synthetic or vector sequence as microbial or human reads as viral. We attribute the high numbers of false positive and false negative calls to a limited reference database with inadequate representation of known diversity. Our comparisons with real world samples show that LMAT-ML is the only tool tested that classifies the majority of reads, and does so with high accuracy.