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Exact(10)
Both strains were identified as P. antarctica, and they were named NRL-A and NRL-B.
Both strains were identified to be K. ohmeri upon partial sequencing.
Both strains were identified as M. intracellulare.
Both strains were identified by Vitek-32 (BioMerieux, Marcy, France).
However, ts alleles of both strains were identified as hits in our screen.
One gene, ADA2, was represented twice in the deletion pool and both strains were identified in our screen.
Similar(50)
The nearest relative to both strains was identified by the N2 sequence of A/mallard/MN/1/2000 (96% nucleotide similarity).
Both virus strains were identified as WNV by complement fixation and neutralization tests (11, 13 ).
Both VB2 and XD4 strains were identified from 4 h SCRaMbLE reactions followed by screening of randomly picked colonies.
Those amino acid residues with an entropy value between 0 and –0.4 for both the human and avian strains were identified as most highly conserved.
Seven strains were identified with both iceA alleles (7 strains, 9.3%).
More suggestions(17)
both species were identified
both cases were identified
both sites were identified
both flavonoids were identified
both alleles were identified
both partners were identified
both strains were observed
both cities were identified
both classrooms were identified
both hits were identified
both patients were identified
both approaches were identified
both groups were identified
both FPs were identified
both populations were identified
both platforms were identified
both strains were sequenced
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