John R. Barnes

Dr. John R. Barnes


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 July 2009 in Science
Verified
Journal Article
Closed access
PDF file
RGRebecca J. Garten
Rebecca J. Garten
CDC. Todd Davis
C. Todd Davis
CRColin Russell
Colin Russell
BSBo Shu
Bo Shu
SLStephen Lindstrom
Stephen Lindstrom
NCNancy J. Cox
Nancy J. Cox
Generation of Swine Flu: As the newly emerged influenza virus starts its journey to infect the world's human population, the genetic secrets of the 2009 outbreak of swine influenza A(H1N1) are being revealed. In extensive phylogenetic analyses, Garten et al. (p. 197 , published online 22 May) confirm that of the eight elements of the virus, the basic components encoded by the hemagglutinin, nucleoprotein, and nonstructural genes originated in birds and transferred to pigs in 1918. Subsequently, these formed a triple reassortant with the RNA polymerase PB1 that transferred from birds in 1968 to humans and then to pigs in 1998, coupled with RNA polymerases PA and PB2 that transferred from birds to pigs in 1998. The neuraminidase and matrix protein genes that complete the virus came from birds and entered pigs in 1979. The analysis offers insights into drug susceptibility and virulence, as well as raising the possibility of hitherto unknown factors determining host specificity. A significant question is, what is the potential for the H1 component of the current seasonal flu vaccine to act as a booster? Apart from the need for ongoing sequencing to monitor for the emergence of new reassortants, future pig populations need to be closely monitored for emerging influenza viruses.

5 September 2016 in BMC Genomics
Verified
Journal Article
Open access
PDF file
SSSamuel S. Shepard
Samuel S. Shepard
SMSarah Meno
Sarah Meno
JBJustin Bahl
Justin Bahl
MWMalania M. Wilson
Malania M. Wilson
JBJohn R. Barnes
John R. Barnes
ENElizabeth Neuhaus
Elizabeth Neuhaus
Deep sequencing makes it possible to observe low-frequency viral variants and sub-populations with greater accuracy and sensitivity than ever before. Existing platforms can be used to multiplex a large number of samples; however, analysis of the resulting data is complex and involves separating barcoded samples and various read manipulation processes ending in final assembly. Many assembly tools were designed with larger genomes and higher fidelity polymerases in mind and do not perform well with reads derived from highly variable viral genomes. Reference-based assemblers may leave gaps in viral assemblies while de novo assemblers may struggle to assemble unique genomes. The IRMA (iterative refinement meta-assembler) pipeline solves the problem of viral variation by the iterative optimization of read gathering and assembly. As with all reference-based assembly, reads are included in assembly when they match consensus template sets; however, IRMA provides for on-the-fly reference editing, correction, and optional elongation without the need for additional reference selection. This increases both read depth and breadth. IRMA also focuses on quality control, error correction, indel reporting, variant calling and variant phasing. In fact, IRMA’s ability to detect and phase minor variants is one of its most distinguishing features. We have built modules for influenza and ebolavirus. We demonstrate usage and provide calibration data from mixture experiments. Methods for variant calling, phasing, and error estimation/correction have been redesigned to meet the needs of viral genomic sequencing. IRMA provides a robust next-generation sequencing assembly solution that is adapted to the needs and characteristics of viral genomes. The software solves issues related to the genetic diversity of viruses while providing customized variant calling, phasing, and quality control. IRMA is freely available for non-commercial use on Linux and Mac OS X and has been parallelized for high-throughput computing.

8 July 2015 in Nature Biotechnology
Verified
Journal Article
Open access
PDF file
AGAmy S Gargis
Amy S Gargis
LKLisa Kalman
Lisa Kalman
DBDavid P Bick
David P Bick
CSCristina da Silva
Cristina da Silva
DDDavid P Dimmock
David P Dimmock
ILIra M Lubin
Ira M Lubin

1 January 2021 in Emerging Infectious Diseases
Verified
Journal Article
Closed access
PDF file
BSBo Shu
Bo Shu
MKMarie K. Kirby
Marie K. Kirby
WDWilliam G. Davis
William G. Davis
CWChristine Warnes
Christine Warnes
JLJimma Liddell
Jimma Liddell
JBJohn R. Barnes
John R. Barnes
RT-PCR for Influenza Viruses and SARS-CoV-2

16 February 2018 in MMWR. Morbidity and Mortality Weekly Report
Verified
Journal Article
Open access
BFBrendan Flannery
Brendan Flannery
JCJessie R. Chung
Jessie R. Chung
EBEdward A. Belongia
Edward A. Belongia
HMHuong Q. McLean
Huong Q. McLean
MGManjusha Gaglani
Manjusha Gaglani
AFAlicia M. Fry
Alicia M. Fry
Although influenza vaccines are the best tool for prevention of influenza currently available, more effective vaccines are needed.

26 September 2018 in Scientific Reports
Verified
Journal Article
Open access
PDF file
MKMatthew W. Keller
Matthew W. Keller
BRBenjamin L. Rambo-Martin
Benjamin L. Rambo-Martin
MWMalania M. Wilson
Malania M. Wilson
CRCallie A. Ridenour
Callie A. Ridenour
SSSamuel S. Shepard
Samuel S. Shepard
JBJohn R. Barnes
John R. Barnes
For the first time, a coding complete genome of an RNA virus has been sequenced in its original form. Previously, RNA was sequenced by the chemical degradation of radiolabeled RNA, a difficult method that produced only short sequences. Instead, RNA has usually been sequenced indirectly by copying it into cDNA, which is often amplified to dsDNA by PCR and subsequently analyzed using a variety of DNA sequencing methods. We designed an adapter to short highly conserved termini of the influenza A virus genome to target the (-) sense RNA into a protein nanopore on the Oxford Nanopore MinION sequencing platform. Utilizing this method with total RNA extracted from the allantoic fluid of influenza rA/Puerto Rico/8/1934 (H1N1) virus infected chicken eggs (EID50 6.8 × 109), we demonstrate successful sequencing of the coding complete influenza A virus genome with 100% nucleotide coverage, 99% consensus identity, and 99% of reads mapped to influenza A virus. By utilizing the same methodology one can redesign the adapter in order to expand the targets to include viral mRNA and (+) sense cRNA, which are essential to the viral life cycle, or other pathogens. This approach also has the potential to identify and quantify splice variants and base modifications, which are not practically measurable with current methods.