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The algorithm presumes that the expressions of the individual genes of the database were measured at the same time points.
Baseline socio-demographic characteristics from the LISA database were measured at the end of 2004 and categorized as shown in Table 1.
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The number of correct and confident identifications (ccID) of the mark matched to a reference database is measured w.r.t. the image capture device and EVA parameters [3].
Each purchased standard compound for compiling into the database was measured by NMR under standardized conditions.
Moreover, since equilibrium constants in the NIST-TECR database are measured in a variety of pH and ionic strength levels, it is difficult to extrapolate the equilibrium constant for the conditions prevailing in an organism or system of interest.
The poverty status for all individuals in the database was measured as of the 1990 census in terms of the ratio of the family income to the poverty threshold for a four-person family and grouped into ≤100%, 100 to <200%, 200 to <400%, 400 to <600%, and 600% or above.
Specifically, biological process, cellular component and molecular function categories were scored with respect to the number of genes included in the Rattus norvegicus database that were measured in the microarray and the number of genes significantly affected by TNBS colitis in each category.
There, data were entered to an SPSS database and error rates were measured on a 10% random sample and found to be below 1%.
The database included the individuals who were measured and weighed on both follow-ups, in accordance with the exclusion criteria established for the 2004 5 follow-up (physically and/or mentally disabled, Down syndrome, and women who were pregnant or had given birth up to three months prior to the interview), for a total of 3739 individuals.
To this end, all known genes localised within the 5 Mb amplicon at 17q23 were obtained from publicly available databases and their expression levels were measured in 26 primary breast tumours using quantitative real-time reverse transcriptase-polymerase chain reaction (qRT-PCR).
Data transfer rates were measured from a local database to a cloud database, results measured were between 125 to 156 ms.
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CEO of Professional Science Editing for Scientists @ prosciediting.com