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The absence of remaining DNA traces was evaluated by quantitative PCR (SDS 7700; Applied Biosystems, Framing-ham, MA) with assays specific for 16s rRNA [ 53, 65].
After additional DNase treatment, the absence of remaining DNA traces was evaluated by quantitative PCR (SDS 7700; Applied Biosystems, Framingham, MA) with assays specific for 16s rRNA and the HU genes [ 32, 70], encoding for a DNA-binding protein.
After additional DNase treatment, the absence of remaining DNA traces was evaluated by quantitative PCR (SDS 7700; Applied Biosystems, Framingham, MA) with assays specific for 16s rRNA [ 63, 64].
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Slip line traces were evaluated in the EBSD micrographs in correlation with the grain orientation.
The underlying mechanism of eligibility traces is evaluated in terms of on-policy and off-policy procedures, as well as accumulating traces and replacing traces.
Risk factors for death before and after patient tracing were evaluated using Cox proportional hazards models after testing the validity of the proportional hazards assumption[6], [8].
The y− trace is evaluated at (t − ϵ), so that the value of the respective synaptic trace is readout before being updated.
The influence of anthropogenic and natural variables on the distribution of trace elements was evaluated, with the proportions of background and anthropogenic sources identified using stochastic models.
The fate of nine trace organic compounds was evaluated during a 12 month large-scale laboratory column experiment.
The correlation of Ca content and trace element levels was evaluated using data obtained from all mineralized bone matrix ROIs (yellow labeled regions in Fig. 2) of all samples.
Further, The electrocatalytic detection performance of the 3D simultaneously reduced and self-assembled sensing architecture (GN-CD-cMWCNT) with trace amounts of CDs was evaluated.
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