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Regulatory DNA was defined to be 250 bases upstream of the +1 start site of an operon or single transcription unit.
Nonfunctional DNA was defined as sequence located between adjacent genes transcribed in convergent directions, which is not expected to contain promoter elements.
Input DNA was defined as an aliquot of sheared chromatin prior to immunoprecipitation, and was used to normalize the amount of chromatin used in each experiment.
High degree of microsatellite instability (MSI-H) in tumor DNA, as compared to corresponding normal DNA, was defined if two or more markers showed aberrant peak profile after fragment analysis.
MRSA DNA was defined using real-time polymerase chain reaction (PCR) with fluorescent hybridization probes.
Intergenic DNA was defined as the sequence not annotated as harboring an RNA or protein-coding gene.
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The complexes they form with DNA are defined as "lipoplexes" or "polyplexes, respectively, and constitute the most promising alternative to the use of viral vectors for gene therapy.
Tester DNA is defined as that in which the differences are being sought relative to a driver DNA.
Tumours with instability at one or two markers compared with germline DNA were defined as MSI-L.
The melting temperature (Tm) of DNA is defined as the temperature at which 50% of double strand becomes single stranded.
Tumours with instability at ⩾3 of the six mononucleotide markers compared with the germline DNA were defined as MSI-H.
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