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The image of the gel was captured and the banding pattern was analyzed using Gelcompar II software (Applied-Maths, Kortrijk, Belgium) and the dendrogram was generated.
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Chromosome numbers were counted in 50 cells (mode analysis), and then the G-band pattern was analyzed in detail in 20 of the cells to identify chromosome aberrations (karyotype analysis).
The DGGE banding patterns were analyzed using Gelcompar II software (version 1.61; Applied Maths, Woluwe, Belgium) to allow comparison of the gels.
Banding patterns were analyzed visually.
Banding patterns were analyzed with BioNumerics software, version 5.0 (Belgium).
The chromosome number and banding patterns were analyzed with a 300 500 band resolution.
Banding patterns were analyzed by using BioNumerics software version 6.01 (Applied Maths, Sint-Martens-Latem, Belgium).
The banding patterns were analyzed by the BioNumerics software (Applied Math, Sint-Maten-Latem, Belgium).
Banding patterns were analyzed by using BioNumerics software version 2.5 (Applied Maths, Sint-Martens-Latem, Belgium).
PFGE banding patterns were analyzed with the Molecular Analyst software (BioRad) using Dice coefficient and UPGMA (unweighted pair group method with arithmetic averages) algorithm.
Banding patterns were analyzed using Image 3.10b and FPC (Fingerprinted Contigs) V6 software [ 61] to assemble overlapping BACs into contigs [ 62].
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