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In our previous study [12], we analyzed mRNA transcripts in breast cancer cell lines and cancer specimens using data sets derived from massively parallel signature sequencing (MPSS) and publicly available expression microarray data.
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The total applied failure load, 2P u, and the corresponding mid-span deflection for each of the beam specimens were recorded using data logger.
The characteristics of the index GWAS on the basis of which investigators were selected are shown in Table 2. Almost two-thirds of respondents reported that their study included primary collection of data and specimens, whereas 37% reported conducting secondary analyses using data and specimens obtained from another investigator or from a repository.
The virtual specimen generator is illustrated using data for an angle interlock weave.
The virtual specimen generator is illustrated using data for an angle interlock weave, a common 3D textile architecture.
This study found a proportion of former study participants are opposed to submitting their genetic and health data to the NIH supported dbGaP database, which suggests these re-consent efforts may be worthwhile and ethically necessary when using data and specimens from past studies.
A formula for α ij was proposed using data obtained from long and short specimens.
We distinguished structural and morphological changes on intact cellular specimens using four-electrode data modeling.
[4] Application of these criteria allows for reliable diagnosis of CAA in living subjects in the absence of cortical biopsy specimens, using clinical and neuroimaging data to assign patients to different groups, based on the likelihood of CAA pathology being present (Table 1).
However, in order to systematically explore relationships and breeding patterns from wild specimens using whole genome sequencing data, high quality DNA is required and in most field studies, non-invasive samples such as feces or hair are used, and the amount of DNA extracted from such samples precludes the application of this methodology to conservation studies.
We further verified miR-133a expression in fresh breast tissue specimens using qRT-PCR and the data confirmed our in situ hybridization data, i.e., miR-133a expression level was significantly lower in breast cancer compared with benign breast disease (P < 0.01; Figure 1D).
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