Exact(1)
Filtering for ER + and HER2- status using array determinations eliminated another 140 samples (51 ER-, 72 HER2+, 17 ER-/HER2+, Additional file 1: Figure S1).
Similar(59)
Analysis of data generated by gene array analysis, determination of intrahepatic cellular origin of transcript expression, and studies of intrahepatic gene expression using gene array analysis are also reviewed.
This study is devoted to creation of metal oxide semiconductor (MOS) materials for gas sensor array for determination of nitrogen oxides and ammonia traces in sub-Threshold Limit Value (TLV) concentrations in air, and to elaboration of data processing algorithms for identification and quantification of single gases.
In such cases, both the clinical and array-based determinations were required to be positive for inclusion in further analysis.
This model has been validated by legacy data, experimental phenotypic arrays, selective determination of metabolites, and growth profiles on defined minimal media.
Some ER- samples were from the Schmidt (2008) dataset (31/201) which did not provide clinical ER status and thus for that study we relied solely on arrays for determination of ER status.
Given the small but significant number of discrepancies observed between clinical and array-based determination of ER status we also recommend inclusion of standard biomarkers such as ER, PR, and HER2 on any design.
Gene expression analysis was performed using a Mouse Multiple Sclerosis RT² Profiler PCR Array, and further determinations and validations of the identified genes were performed using qPCR.
For our studies, we used SNP array data for determinations of tumor cell DNA percentages.
The comparison of the sensor array with HPLC determination of the carboxylic acids was finally made.
In this work, an amperometric biosensor array for simultaneous determination of ethanol, formate, d- and l-lactate is presented.
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