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Tester DNA is defined as that in which the differences are being sought relative to a driver DNA.
The melting temperature (Tm) of DNA is defined as the temperature at which 50% of double strand becomes single stranded.
Chromatin configuration in different regions of the genome, such as promoters, enhancers, and those of transcribed DNA, is defined by distinct histone modification patterns [ 32].
Selfish DNA is defined as a segment of the genome with no apparent function other than to ensure its own replication.
A titration of RepD into a solution of Junction 1 (DNA is defined in Figure 2) is shown in Figure 3a.
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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.
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.
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