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Plant Virology Protocols

Overview of attention for book
Cover of 'Plant Virology Protocols'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Detection of Plant Viruses in Mixed Infection by a Macroarray-Assisted Method
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    Chapter 2 Rt-PCR and real-time rt-PCR methods for the detection of potato virus y in potato leaves and tubers.
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    Chapter 3 A New Method to Isolate Total dsRNA
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    Chapter 4 Multiplex RT-PCR Method for the Simultaneous Detection of Nine Grapevine Viruses
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    Chapter 5 Detection Methods for Rice Viruses by a Reverse-Transcription Loop-Mediated Isothermal Amplification (RT-LAMP).
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    Chapter 6 Real-Time PCR Protocols for the Quantification of the Begomovirus Tomato Yellow Leaf Curl Sardinia Virus in Tomato Plants and in Its Insect Vector
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    Chapter 7 Detection and Analysis of Non-retroviral RNA Virus-Like Elements in Plant, Fungal, and Insect Genomes.
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    Chapter 8 Detection of Plant Viruses in Natural Environments by Using RNA-Seq
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    Chapter 9 Cloning and Profiling of Small RNAs from Cucumber Mosaic Virus Satellite RNA
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    Chapter 10 Drawing siRNAs of Viral Origin Out from Plant siRNAs Libraries.
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    Chapter 11 Viral detection by high-throughput sequencing.
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    Chapter 12 Plant Virology Protocols
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    Chapter 13 Detection and characterization of mycoviruses in arbuscular mycorrhizal fungi by deep-sequencing.
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    Chapter 14 SuperSAGE as an Analytical Tool for Host and Viral Gene Expression.
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    Chapter 15 Microarray Analysis of R -Gene-Mediated Resistance to Viruses
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    Chapter 16 Construction of Infectious cDNA Clones Derived from the Potyviruses Clover Yellow Vein Virus and Bean Yellow Mosaic Virus
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    Chapter 17 Virus-Induced Gene Silencing of N Gene in Tobacco by Apple Latent Spherical Virus Vectors
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    Chapter 18 Simplified Methods for the Construction of RNA and DNA Virus Infectious Clones
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    Chapter 19 Efficient double-stranded RNA production methods for utilization in plant virus control.
  21. Altmetric Badge
    Chapter 20 Detection of plant virus in meristem by immunohistochemistry and in situ hybridization.
Attention for Chapter 8: Detection of Plant Viruses in Natural Environments by Using RNA-Seq
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (86th percentile)
  • High Attention Score compared to outputs of the same age and source (95th percentile)

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Citations

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Chapter title
Detection of Plant Viruses in Natural Environments by Using RNA-Seq
Chapter number 8
Book title
Plant Virology Protocols
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-1743-3_8
Pubmed ID
Book ISBNs
978-1-4939-1742-6, 978-1-4939-1743-3
Authors

Atsushi J Nagano, Mie N Honjo, Motohiro Mihara, Masanao Sato, Hiroshi Kudoh, Atsushi J. Nagano, Mie N. Honjo, Nagano, Atsushi J., Honjo, Mie N., Mihara, Motohiro, Sato, Masanao, Kudoh, Hiroshi

Abstract

Sequencing of RNA by next generation sequencers, RNA-Seq, is revolutionizing virus detection. In addition to the unbiased detection of various viruses from wild plants in natural environments, RNA-Seq also allows for the parallel collection of host plant transcriptome data. Host transcriptome data are highly valuable for studying the responses of hosts to viral infections, as well as viral host manipulation. When detecting viruses using RNA-Seq, it is critical to choose appropriate methods for the removal of rRNA from total RNA. Although viruses with polyadenylated genomes can be detected by RNA-Seq following mRNA purification using oligo-dT beads, viruses with non-polyadenylated genomes are not effectively detected. However, such viruses can be detected by RNA-Seq using the rRNA selective depression method. The high-throughput and cost-effective method of RNA-Seq library preparation which is described here allows us to detect a broad range of viruses in wild plants.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 2%
Switzerland 1 2%
Unknown 53 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 10 18%
Student > Bachelor 9 16%
Student > Doctoral Student 8 15%
Student > Ph. D. Student 7 13%
Other 4 7%
Other 12 22%
Unknown 5 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 30 55%
Biochemistry, Genetics and Molecular Biology 8 15%
Computer Science 2 4%
Social Sciences 2 4%
Chemical Engineering 1 2%
Other 4 7%
Unknown 8 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 10. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 10 October 2014.
All research outputs
#3,250,899
of 22,765,347 outputs
Outputs from Methods in molecular biology
#788
of 13,090 outputs
Outputs of similar age
#48,583
of 352,893 outputs
Outputs of similar age from Methods in molecular biology
#44
of 996 outputs
Altmetric has tracked 22,765,347 research outputs across all sources so far. Compared to these this one has done well and is in the 85th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,090 research outputs from this source. They receive a mean Attention Score of 3.3. This one has done particularly well, scoring higher than 93% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 352,893 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 86% of its contemporaries.
We're also able to compare this research output to 996 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 95% of its contemporaries.