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This book deals with the first discriminant theory of linearly separable data (LSD), Theory3, based on the four ordinary LSD of Theory1 and 169 microarrays (LSD) of Theory2. Furthermore, you can quickly analyze the medical data with the misclassified patients which is the true purpose of diagnoses. Author developed RIP (Optimal-linear discriminant function finding the combinatorial optimal solution) as Theory1 in decades ago, that found the minimum misclassifications. RIP discriminated 63 (=26¿1) models of Swiss banknote (200*6) and found the minimum LSD: basic gene set (BGS). In Theory2, RIP discriminated Shipp microarray (77*7129) which was LSD and had only 32 nonzero coefficients (first Small Matryoshka; SM1). Because RIP discriminated another 7,097 genes and found SM2, the author developed the Matryoshka feature selection Method 2 (Program 3), that splits microarray into many SMs. Program4 can split microarray into many BGSs. Then, the wide columnLSD (Revolution-0), such as microarray (n5) models, including BGS, become LSD among (219¿1) models. Because Program2 confirms BGS has the minimum average error rate, BGS is the most compact and best model satisfying Occam¿s Razor. With this book, physicians obtain complete diagnostic results for disease, and engineers can become a true data scientist, by obtaining integral knowledge ofstatistics and mathematical programming with simple programs.
This book shows how to decompose high-dimensional microarrays into small subspaces (Small Matryoshkas, SMs), statistically analyze them, and perform cancer gene diagnosis.
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