| 摘要 |
Various embodiments of the present invention determine a zero point, or centralization constant zeta, for an array-based comparative genomic hybridization ("aCGH") data set by identifying a zero-point value, or centralization constant zeta, that, when used in an aberration-calling analysis of the aCGH data, results in the fewest number of array-probe-complementary genomic sequences identified as having abnormal copy numbers with respect to a control genome, or, in other words, results in the greatest number of array-probe-complementary genomic sequences identified as having normal copy numbers. In one embodiment, interval-based analysis of an aCGH data set may be carried out using a range of putative zero-point values, and the zero-point value for which the maximum number of genomic sequences are determined to have normal copy numbers may then be selected.
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