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. 2009 Jul;11(7):1728–1735. doi: 10.1111/j.1462-2920.2009.01899.x

Table 2.

Peak-to-peak correlation (as a percentage of total OTUs) between measured TRFLP patterns and predicted TRFLP patterns from an in silico digestion of 16S rRNA clone library data.

South Rift
Pisces Peak
15 f.u. cut-off 50 f.u. cut-off 15 f.u. cut-off 50 f.u. cut-off
TRFLP peaks perfect match 12 ± 4 8 ± 10 42 ± 4 56 ± 11
TRFLP peaks off by 1–2 bp 25 ± 13 37 ± 29 30 ± 4 32 ± 12
TRFLP peaks not matched 63 ± 12 55 ± 20 28 ± 3 12 ± 7
TRFLP ‘members’ identified 67 ± 11 75 ± 9 92 ± 3 93 ± 3
in silico peaks perfect match 24 ± 13 6 ± 8 29 ± 4 15 ± 4
in silico peaks off by 1–2 bp 45 ± 15 20 ± 15 21 ± 4 8 ± 3
in silico peaks not matched 30 ± 7 77 ± 3 50 ± 6 77 ± 3

Data are presented for the correlations when the measured TRFLP fragments are assumed versus both 15- and 50-fluorescence-unit (f.u.) threshold cut-off values.