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. 2004 Mar;70(3):1455–1465. doi: 10.1128/AEM.70.3.1455-1465.2004

TABLE 3.

Summary information for the six probes yielding the highest signals when the CBv1 array was hybridized with a target derived from a natural Chesapeake Bay picoplankton community

Clone (probe locationa) Signal (% of peak) Closest match (GenBank accession no.)b % Similarityc
CB914H3 (D11) 100 Uncultivated; clone NRS1C607 from Neuse River Estuary (AF518561) 91 (323/327)
CB916H3 (G6) 74 Uncultivated; clone SIS2-7 from decaying sea grass (AF389736) 89 (321/327)
CB894H6 (B9) 50 Uncultivated; clone g1-HW4 from soil (AY196408) 89 (327/327)
CB910H3 (A7) 48 Uncultivated; clone SIS2-7 from decaying sea grass (AF389736) 88 (320/327)
CB907H10 (D8) 30 Bradyrhizobium sp. strain IRBG 230 (AB079617) 96 (194/324)
CB907H9 (E5) 26 Uncultivated; clone nifH51 from sweet potato (AY159593) 94 (324/324)
a

Array location (as in Fig. 3).

b

The most similar sequence in GenBank as determined by the BLAST algorithm (2).

c

Similarities between the probe and the top-ranked BLAST match are presented as a percentage followed, in parentheses, by the ratio of the length of the matching region to the total length of the submitted fragment.