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Below, we demonstrate this protocol for ChIP enrichment using mouse chromosome 16 tiling microarrays (Agilent Technologies), followed by subsequent deep sequencing using an Illumina/Solexa 1G Genome Analyzer.
Below, we demonstrate that this estimate accurately reflects the fluid conditions inside the channel, and that by adjusting the position of the interface, time-varying chemical signals can be generated and applied to living cells, and their responses observed.
Below, we demonstrate that forming such bridges is of fundamental importance, especially if it can be achieved at the level of individual trials.
Below, we demonstrate the utility of ProKinO in cancer kinome mining and annotation using the knowledge conceptualized on conserved motifs associated with kinase function and regulation.
In contrast, based on the theatrical analyses and empirical results presented below, we demonstrate that the MV, selected by the proposed motion estimation process, is less affected by QP.
In the experiments below, we demonstrate just this.
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Below, we first demonstrate the accuracy of our performance model in Section 6.1 and then verify our optimization result in Section 6.2.
As we demonstrate below, the organization of video into sequences allows a more efficient use of the available memory resources in comparison to the widely used classical division of the videos into segments of equal size.
As we demonstrate below, one cannot differentiate these views on the basis of data collected by conventional means because all three can produce equivalent effects when only a single independent variable is manipulated.
However, as we demonstrate below, a subset of these polymorphisms do affect splicing efficiency.
As we demonstrate below, the observed current fluctuations are dependent on the concentration of the Hsc70 present in solution.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com