Evidence map›Paper›PMID 20961419›Full record

ArticleBMC genomics2010

Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigm.

India Leclercq, Nicolas Berthet, Christophe Batéjat, Claudine Rousseaux, Philip Dickinson, Iain G Old, Katherine Kong, Giulia C Kennedy, Stewart T Cole, Jean-Claude Manuguerra

Abstract read
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

India LeclercqInstitut Pasteur, Laboratory for Urgent Response to Biological Threats (CIBU), Paris, France.
Nicolas Berthet
Christophe Batéjat
Claudine Rousseaux
Philip Dickinson
Iain G Old
Katherine Kong
Giulia C Kennedy
Stewart T Cole
Jean-Claude Manuguerra

Funding

Pathogen and Genetic Element Detection Using MicroarraysUC1AI062613 · NIAID · AFFYMETRIX, INC. · PI KENNEDY, GUILIA C · 2004 to 2004
$2.1M
6 · The paper itself

Abstract

backgroundA resequencing microarray called PathogenID v2.0 has been developed and used to explore various strategies of sequence selection for its design. The part dedicated to influenza viruses was based on consensus sequences specific for one gene generated from global alignments of a large number of influenza virus sequences available in databanks.

resultsFor each HA (H1, H2, H3, H5, H7 and H9) and NA (N1, N2 and N7) molecular type chosen to be tested, 1 to 3 consensus sequences were computed and tiled on the microarray. A total of 12 influenza virus samples from different host origins (humans, pigs, horses and birds) and isolated over a period of about 50 years were used in this study. Influenza viruses were correctly identified, and in most cases with the accurate information of the time of their emergence.

conclusionsPathogenID v2.0 microarray demonstrated its ability to type and subtype influenza viruses, often to the level of viral variants, with a minimum number of tiled sequences. This validated the strategy of using consensus sequences, which do not exist in nature, for our microarray design. The versatility, rapidity and high discriminatory power of the PathogenID v2.0 microarray could prove critical to detect and identify viral genome reassortment events resulting in a novel virus with epidemic or pandemic potential and therefore assist health authorities to make efficient decisions about patient treatment and outbreak management.

Indexed as

AnimalsBase SequenceBirdsConsensus SequenceHumansInfluenza A virusInfluenza, HumanInfluenza in BirdsOligonucleotide Array Sequence AnalysisRNA, ViralSequence Analysis, DNARNA, Viral

Identifiers

PMID20961419
PMCPMC3091733

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.