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All SNPs were genotyped using the TaqMan platform (Applied Biosystems) according to manufacturer's protocols.
Genotypes were called using the proprietary software supplied by Illumina (BeadStudio, version 3.1.3).. Validation set genotyping was carried out using the TaqMan platform according to the manufacturer's protocol (Applied Biosystems, Foster City, CA, USA).
Genotyping was performed using the Taqman platform (Life Technologies).
Genotyping was carried out using the TaqMan platform following the manufacturer's instructions.
Genotyping was carried out using the TaqMan platform as per the manufacturer's instructions.
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In addition, 7 other microRNAs (hsa-miR-155, hsa-miR-15a, hsa-miR-17, hsa-miR-20a, hsa-miR-20b, hsa-miR-34a, hsa-miR-93) were chosen for qPCR confirmation of array data using the Taqman qPCR platform (Life Technologies).
Gene expression analysis was performed using the Taqman Low Density Array platform.
Genotypes were determined using the Taqman allelic discrimination assay.
To quantify the miR156 and miR172 expression, PCR was performed using the TaqMan Fast Universal PCR Master Mix (Applied Biosystem).
We genotyped SNPs using the TaqMan assay.
PCR products were amplified from each cDNA sample using the TaqMan MicroRNA Assay together with the TaqMan® Universal PCR Master Mix.
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