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Mutation analysis was performed simultaneously.
Mutation analysis was performed to evaluate the capabilities of the test cases to detect faults.
No patient selection based on mutation analysis was performed at the time of approval and all eligible NSCLC patients were treated with erlotinib [14].
IGHV mutation analysis was performed by multiplex PCR using the BIOMED2 protocol.
Mutation analysis was performed by direct sequencing using the Big Dye Terminator Protocol.
Gene conversion and mutation analysis was performed as described previously [13].
Mutation analysis was performed by sequencing of the complete coding sequences of the genes and analysis of all mutations on both genomic gene fragments and transcripts.
Biomarker mutation analysis was performed.
bSomatic mutation analysis was optional.
DNA mutation analysis was 100% concordant between two laboratories.
Mutation analysis was performed by PCR-DHPLC analysis.
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