Global ETD Search
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Showing 1 to 2 of 2 for “"Array Comparative genomic hybridization (ACGH)"”.
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IDENTIFICATION OF LOCI CONTRIBUTING TO THE SMITH-MAGENIS SYNDROME-LIKE PHENOTYPE AND MOLECULAR EVALUATION OF THE RETINOIC ACID INDUCED 1 GENE
… all SMS-like subjects were sent for whole genome array comparative genomic hybridization (aCGH) to identify duplications or deletions of each individual’s genome which contribute to the phenotype observed. We identified 6 pathogenic copy number variants (CNVs) in six individuals which contribute …
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Bayesian Latent Class Models
… into the clustering of the breast cancer microarray data. In the last part of this paper, our future work is represented.