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However, for DNA RM [8] development, basic research of quantification methods was needed, in order to study the consistency of these methods and analyse the uncertainty sources [9].
SSCP and RFLP, the most widely used techniques for mutation screening method in genetic diagnostic laboratories, were not able to detect every mutation, so development of new methods was needed.
Since significant interlaboratory variation was observed worldwide, it was internationally confirmed that calibration traceability to higher-order reference methods was needed to realize comparable biochemical measurement results [ 2, 6, 7].
Similar(57)
Bigger GWAS, with more statistical power, may help a bit, but clearly new methods are needed.
Other methods are needed.
Therefore, alternative strengthening methods are needed.
Therefore, different control methods are needed.
Therefore, robust synchronization methods are needed.
Heuristic methods are needed for larger instances.
Thus, faster, more reliable methods are needed.
Unified and aligned working methods are needed.
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