Sentence examples for the specimens were analysed using from inspiring English sources

The specimens were analysed using Flow Cytometry at 620 nm.

The specimens were analysed using nucleic acid amplification tests utilising target capture, transcription-mediated amplification and hybridisation protection assays.

The fracture surfaces of the tensile specimens were analysed using SEM to reveal the mode of fracture.

The stained specimens were analysed using Zeiss (Oberkochen, Germany) Axiovert 200 ℳ microscope equipped with Yokogawa (Tokyo, Japan) CSU22 confocal scanner unit and Intelligent Imaging Innovations (Intelligent Imaging Innovations, Inc., Denver, CO, USA) laser unit microscope using 63 × oil objective.

The RNA from FFPE breast tumour specimens were analysed using the DASL assay.

Data obtained from immunohistochemistry on patient specimens were analysed using the non-parametric Wilcoxon matched pairs t test.

Central hole notched specimens were analysed using a fracture mechanics approach.

All specimens were analysed using enzyme immunoassay test.

For diagnosis of N gonorrhoeae and C trachomatis, endocervical specimens were analysed using AMPLICOR CT/NG PCR (Roche Diagnostics, Indianapolis, USA), including AMPLICOR Neisseria gonorrhoeae Detection Kit and AMPLICOR Chlamydia trachomatis Detection Kit, in accordance with the instructions of the manufacturer.

Specimens were analysed using a general primer GP5+/GP6+-based polymerase chain reaction and genotyped for 18 high-risk and 6 low-risk HPV- strains by Luminex-based multiplexed genotyping.

A total of 783 breast cancer specimens were analysed using a tissue microarray; of which 58.1% (455/783) were invasive ductal carcinomas, 17.0% (133/783) were tubular mixed, 6.5% (51/783) were classic lobular, all other subcategories accounted for less than 5% of the studied cohort.