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The Onco type DX Breast Cancer Assay (Genomic Health, Redwood City, CA, USA) and the MammaPrint diagnostic test (Agendia, Irvine, CA, USA) were the first commercially available gene expression tests to predict the risk of recurrence in early-stage BC [ 1- 3].
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The classifier genes identified in this study, and validated by TaqMan® real-time PCR, define a set of promising potential diagnostic markers, setting the stage for a blood-based gene expression test to facilitate early detection of TAA.
EndoPredict (EP) is a clinically validated multianalyte gene expression test to predict distant metastasis in ER-positive, HER2-negative breast cancer treated with endocrine therapy alone.
To assess whether a variant may influence the expression of a nearby gene, a variety of in silico databases are available that allow a gene expression test to be performed.
We envisage blood-based gene-expression tests to have the potential of becoming a versatile and powerful tool for detection of disease, including other forms of cancers.
The sequencing data (fastq files), the gene expression pattern of all samples (output file of Cufflinks "gene expression" converted to Excel) and the results (output file of Cuffcompare "gene differential expression testing" converted to Excel) are uploaded to the NCBI, GEO under the accession number GSE4148.
The tools include a variety of rule-processing classes that allow an algorithm to direct the way in which language is assessed, from basic pertinent expression existence tests, to the assignment and assessment of Bayesian probabilities.
Oil expression tests were conducted to evaluate the performance of a novel oil expeller designed and fabricated to operate on a 200 W solar photovoltaic (PV) power system as a sole power source.
Since 2009, the St Gallen International breast cancer panel has recognized both the robustness of validated gene expression tests and their ability to add prognostic information to clinicopathological factors [ 7].
Moreover, Caspase-3 expression tests were only meant to act as supplemental indications of cell death, rather than relying on statistical analysis of the data for definitive conclusions.
The expression of calpain-1, calpain-2 and calpastatin cytoplasmic and nuclear expression was tested to determine associations with clinicopathological criteria in the pancreatic and the grouped bile duct and ampullary cancers.
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