See Figure 2 for sample scans of oligonucleotide hybridisations, which reveal the spotting patterns.
For comparative analysis of protein expression in embryos or cells through confocal microscopy, the auto gain function was switched off and the same gain and photomutiplier settings were used for each sample scanned and analyzed.
To avoid the random error in detection, each sample was scanned for three times.
Reference lists of all papers included in the final sample were scanned for any additional relevant papers.
Ten undamaged leaves were taken from each branch sample and scanned for image analysis conducted with LAMINA [ 59] to obtain leaf area.
The radiographs, urine samples, and MRI scans for this study were acquired at baseline (BL) and at follow-up after 21 months (FU).
The samples are scanned for 2θ angle from 10 to 80 degrees.
When these same samples were scanned for amino sugars, the presence of QuiNAc, GalNAc, and GlcNAc was also confirmed.
All samples were scanned for c.563C > T mutation and c.1311C > T polymorphism by restriction fragment length polymorphism (PCR-RFLP).
In the final step, all samples are scanned for common fusion predictions to reduce false-positive predictions.
