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Exact(8)
Using their predicted locations, only mutations near nucleotides that could be mutated to potential stop or splice junction mutations were sequenced.
Mutations were sequenced twice from different PCR reactions to verify the aberration.
Suspicious fragments indicating mutations were sequenced on a Licor 4000L sequencing machine.
Four of the five new Cyclin E mutations were sequenced and the predicted protein changes identified (Table 1).
All mutations were sequenced (Genewiz) to confirm that the DNA sequence contained only the desired point mutation.
Most mutations were sequenced in both directions using either the same forward or reverse primers as for PCR or an internal primer designed for sequencing.
Similar(52)
Mutations were sequence-verified.
All deletion mutations are sequenced.
The conventional approach for genotyping RET mutations is sequencing the exons.
The relatively high coverage of our assemblies (Table 1) makes unlikely that disrupting mutations are sequencing errors.
Each mutation was sequenced in reprogrammed clones, and pluripotency was determined by differentiation to each germ layer from embryoid bodies.
More suggestions(15)
transformants were sequenced
times were sequenced
mutations were found
mutations were identified
mutations were selected
mutations were used
mutations were genotyped
mutations were described
mutations were detected
mutations were verified
mutations were eliminated
mutations were analyzed
mutations were inherited
mutations were observed
mutations were confirmed
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