RT Journal Article SR Electronic T1 Rapid metagenomic identification of viral pathogens in clinical samples by real-time nanopore sequencing analysis JF bioRxiv FD Cold Spring Harbor Laboratory SP 020420 DO 10.1101/020420 A1 Alexander L. Greninger A1 Samia N. Naccache A1 Scot Federman A1 Guixia Yu A1 Placide Mbala A1 Vanessa Bres A1 Doug Stryke A1 Jerome Bouquet A1 Sneha Somasekar A1 Jeffrey M. Linnen A1 Roger Dodd A1 Prime Mulembakani A1 Bradley S. Schneider A1 Jean-Jacques Muyembe A1 Susan L. Stramer A1 Charles Y. Chiu YR 2015 UL http://biorxiv.org/content/early/2015/06/05/020420.abstract AB We report unbiased metagenomic detection of chikungunya virus (CHIKV), Ebola virus (EBOV), and hepatitis C virus (HCV) from four human blood samples by MinION nanopore sequencing coupled to a newly developed, web-based pipeline for real-time bioinformatics analysis on a computational server or laptop (MetaPORE). At titers ranging from 107-108 copies per milliliter, reads to EBOV from two patients with acute hemorrhagic fever and CHIKV from an asymptomatic blood donor were detected within 4 to 10 minutes of data acquisition, while lower titer HCV virus (1x105 copies per milliliter) was detected within 40 minutes. Analysis of mapped nanopore reads alone, despite an average individual error rate of 24% [range 8-49%], permitted identification of the correct viral strain in all 4 isolates, and 90% of the genome of CHIKV was recovered with >98% accuracy. Using nanopore sequencing, metagenomic detection of viral pathogens directly from clinical samples was performed within an unprecedented <6 hours sample-to-answer turnaround time and in a timeframe amenable for actionable clinical and public health diagnostics.