pubmed-article:20964857 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C0014346 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C0348026 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C0036576 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C1449575 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C0034980 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C0182400 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C1705938 | lld:lifeskim |
pubmed-article:20964857 | lifeskim:mentions | umls-concept:C1527178 | lld:lifeskim |
pubmed-article:20964857 | pubmed:dateCreated | 2010-11-18 | lld:pubmed |
pubmed-article:20964857 | pubmed:abstractText | The Enterobacteriaceae comprise a large number of clinically relevant species with several individual subspecies. Overlapping virulence-associated gene pools and the high overall genome plasticity often interferes with correct enterobacterial strain typing and risk assessment. Array technology offers a fast, reproducible and standardisable means for bacterial typing and thus provides many advantages for bacterial diagnostics, risk assessment and surveillance. The development of highly discriminative broad-range microbial diagnostic microarrays remains a challenge, because of marked genome plasticity of many bacterial pathogens. | lld:pubmed |
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