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1 housekeeping genes, data were analyzed using Significance Analysis of Microarrays.
2 onses were compared among ABL tertiles using significance analysis of microarrays.
3 size, or mixture distribution of noises than Significance Analysis of Microarrays.
4 ble than those obtained by t-test P value or Significance Analysis of Microarrays.
5 alysis of microarrays and cell type-specific significance analysis of microarrays.
9 mpared with standard metrics, including both significance analysis of microarrays and cell type-speci
10 rays (Affymetrix) and analyzed the data with significance analysis of microarrays and prediction anal
11 hat identify differentially expressed genes (significance analysis of microarrays) and minimal subset
14 red analysis of global gene expression using significance analysis of microarrays detected 48 up-regu
15 contrast, standard analytical tools, such as significance analysis of microarrays, detected a marker
16 ayesian analysis tool was more accurate than significance analysis of microarrays for predicting chec
17 ved in these and our previous experiments by significance analysis of microarrays indicated excellent
18 iation sensitivity as a continuous variable, significance analysis of microarrays is used for gene se
19 ared with their corresponding controls using significance analysis of microarrays (<1% false discover
20 stic by either incorporating the idea of the significance analysis of microarrays method or using the
23 We explore the possibility of applying the Significance Analysis of Microarray (SAM) method (PNAS 9
24 cluding the empirical Bayes (EB) method, the significance analysis of microarray (SAM) method and the
25 cal Bayes method of Efron et al. (2001), the significance analysis of microarray (SAM) method of Tush
26 ical Bayesian method of Efron et al. and the Significance Analysis of Microarray (SAM) method of Tush
27 her level in the flower than the leaf by the Significance Analysis of Microarray (SAM) method with a
31 ession between the five different genotypes, significance analysis of microarrays (SAM) and one-way A
32 rray signal intensities were analyzed by the significance analysis of microarrays (SAM) approach.
34 identified by univariate approaches such as Significance Analysis of Microarrays (SAM) or Linear Mod
35 ctiveness of the proposed procedure with the significance analysis of microarrays (SAM) procedure.
36 The microarray datasets were analyzed with significance analysis of microarrays (SAM) to identify g
37 he bioinformatics software Cluster/TreeView, Significance Analysis of Microarrays (SAM), and ANNs.
39 on Affymetrix GeneChips were analyzed using Significance Analysis of Microarrays (SAM), to determine
40 normal and malignant lesions, as defined by significance analysis of microarrays (SAM), were compare
43 ates and stringent analytic tools, including significance analysis of microarrays to estimate and man
45 lusters of reactivity, and after unblinding, significance analysis of microarrays was used to identif
46 erential gene expression was assessed by the significance analysis of microarrays, with the false-dis
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