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Although moderate-to-good agreement has been reported between the two methods, validation of DNA microarray results by the more sensitive PCR array is generally recommended [38].
To save computational cost, the generalized sidelobe canceller (GSC) is an effective approach generally applied in radar and communication systems where the desired signal is only presented in a fraction of time or the amplitude of the desired signal in the auxiliary array is generally very small [7, 8].
However, in metazoans we observe that each gene sequence in the array is generally the same, producing sequence similarity within a species and sequence diversity between species [ 14, 15].
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A small proportion of the repeats within a given homogeneous alphoid array are generally engaged in the functional centromere [ 16, 17].
For example, for 14-nm node FinFET devices, top CD of fin arrays is generally less than 10 nm, which can be easily fabricated by above methods.
But the fundamental question addressed using arrays is generally a comparison between paired samples to find genes that are significantly different in their patterns of expression.
The variation of the arrays is generally explained by only a small number of factors, of which the first (the major source of variation) represents variation the arrays have in common [ 18, 20- 26, 27, 27].
Arrays are generally probed with soluble lectins or soluble fragments of membrane receptors that have been fluorescently labeled.
The arrays are generally considered easier to use with less complicated and less labor-intensive sample preparation than RNA-Seq.
However, our immune genes, when expressed on the Novartis arrays, are generally clustered in tissues of the immunohematopoietic system, the gastrointestinal tract, and lung.
The crystalline arrays are generally 5 10 nm thick and represent highly porous protein lattices (30 70% porosity) with pores of uniform size and morphology in the 2 8 nm range.
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