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Appl. Environ. Microbiol., 04 1995, 1240-1245, Vol 61, No. 4
JF Robison-Cox, MM Bateson and DM Ward
Detection of chimeric artifacts formed when PCR is used to retrieve
naturally occurring small-subunit (SSU) rRNA sequences may rely on
demonstrating that different sequence domains have different phylogenetic
affiliations. We evaluated the CHECK_CHIMERA method of the Ribosomal
Database Project and another method which we developed, both based on
determining nearest neighbors of different sequence domains, for their
ability to discern artificially generated SSU rRNA chimeras from authentic
Ribosomal Database Project sequences. The reliability of both methods
decreases when the parental sequences which contribute to chimera formation
are more than 82 to 84% similar. Detection is also complicated by the
occurrence of authentic SSU rRNA sequences that behave like chimeras. We
developed a naive statistical test based on CHECK_CHIMERA output and used
it to evaluate previously reported SSU rRNA chimeras. Application of this
test also suggests that chimeras might be formed by retrieving SSU rRNAs as
cDNA. The amount of uncertainty associated with nearest-neighbor analyses
indicates that such tests alone are insufficient and that better methods
are needed.
Copyright © 1995, American Society for Microbiology
Evaluation of nearest-neighbor methods for detection of chimeric small- subunit rRNA sequences
Department of Mathematical Sciences, Montana State University, Bozeman 59717, USA.
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