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DNA patterns were analysed with BioNumerics software (V 6.6, Applied Maths, Sint-Martens-Latem, Belgium).
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DNA ploidy patterns were analysed in multiple samples from each tumour using flow cytometry and compared with clinical stage, tumour invasion, metastatic rate and survival.
The DNA banding patterns were analysed with the use of BioNumerics v. 6.10 software (Applied Maths, Saint-Martens-Latem, Belgium) using Dice coefficient of similarity with band tolerance of 1% and cluster analysis based on the unweighted pair group method with arithmetic averages (UPGMA).
Temporal patterns were analysed by regression techniques.
The response patterns were analysed statistically.
Peak patterns were analysed using the ALFwin Fragment Analyzer Programme (Amersham Biosciences), and shifted peaks were defined as mutations in the respective DNA fragment.
Patients with a dominant inheritance pattern were analysed using MLPA Retinitis Probemix (P235).
A total of 267 patients with NSCLC (pathologically documented stage I, II, or IIIA) underwent complete resection, and DNA ploidy pattern was analysed.
For genotypic characterisation, hybridisation patterns on DNA arrays were analysed.
Alterations within the retinoblastoma (Rb) gene, as detected by the VNTR probe p68RS2.0, and flow cytometric DNA pattern have been analysed in 255 colorectal carcinomas.
Viral loads were measured in samples with detectable HBV DNA and the DNA sequences were analysed.
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