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This array evaluated the expression of 84 genes involved in cell-cell and cell-matrix interactions.
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Each TaqMan Array evaluates two cDNA samples in triplicate generated in a reverse transcription step using random primers.
Hybridization performance of this array was evaluated using Atlantic salmon, rainbow trout, coho salmon, brook trout and lake whitefish RNA obtained from liver organs.
An external validation series by the Transbig consortium using this same customized mini-array, evaluating outcome prediction of 307 patients from 5 European hospitals who were diagnosed with lymph node negative breast cancer before the age of 60 years and who did not receive adjuvant therapy, showed the independent clinical validation of the 70-gene expression profile[ 21].
The samples' quality and percentage of tumor cells were controlled with tissue arrays, evaluating an adjacent tissue piece.
No segregation distortion was detected in this SSR marker array as evaluated by F2 chi-square segregation analyses.
Array performance for the 15K array, was evaluated and validated using RNA materials from P. falciparum clinical isolates.
In this array, the vaccine candidate evaluated was PspA; however, other arrays could include other variable virulence genes.
To evaluate array CGH use for hamster, we co-hybridized genomic DNA from hamster and human to the array and evaluated the signal intensities for each channel separately.
The array was evaluated using multiple primer pairs.
The sensing properties of the sensor array were evaluated inside the quartz pipe.
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