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1 thout the requirement for a priori candidate gene selection.
2 important for reducing bias due to adaptive gene selection.
3 ess the potentially large bias introduced by gene selection.
4 ticipate in conferring specificity of target gene selection.
5 eves effective scRNA-seq data clustering and gene selection.
6 on (QIF) framework was applied for efficient gene selection.
7 sufficient to strongly influence p53 target gene selection.
8 sed using conventional methods for on-target gene selection.
9 WNT/p21 circuit is driven by C-clamp target gene selection.
10 nces in DNA specificities can dictate target gene selection.
11 ce of a differentially expressed pathway and gene selection.
12 thms which represent the stat-of-the-art for gene selection.
13 taneous cluster selection and within cluster gene selection.
16 is crucial to develop a simple but efficient gene selection algorithm for detecting differentially ex
18 we describe a machine learning-based marker gene selection algorithm, NS-Forest version 2.0, which l
20 mplements leading pattern classification and gene selection algorithms and incorporates cross-validat
22 , BLogReg and Relevance Vector Machine (RVM) gene selection algorithms are evaluated over the well-st
24 rion idea of Chen et al., we propose two new gene selection algorithms for general Bayesian models an
27 provide a unified procedure for simultaneous gene selection and cancer classification, achieving high
28 Importantly, the implementation integrates gene selection and class prediction stages, which is vit
29 he Bayesian model averaging (BMA) method for gene selection and classification of microarray data.
32 with the optimum combination of classifier, gene selection and cross-validation methods, we performe
33 self-organizing maps, and modules for marker gene selection and heat map visualization that allow use
36 oys a two-stage manifold fitting process for gene selection and noise reduction, followed by agglomer
39 nome, then reveal tarsier-specific, positive gene selection and posit population size changes over ti
41 cerGenes resource to simplify the process of gene selection and prioritization in large collaborative
42 cells of interest without the constraint of gene selection and the ambiguous nature of data obtained
43 atical programming approach is developed for gene selection and tissue classification using gene expr
44 NA binding, subcellular localization, target gene selection and transcriptional activity of Ets prote
46 Our objective is to understand p53 target gene selection and, thus, enable its optimal manipulatio
47 ificance analysis of microarrays is used for gene selection, and a multivariate linear regression mod
48 nalytic tool, iterative clustering and guide-gene selection, and clonogenic assays to delineate hiera
49 used for gene function prediction, candidate gene selection, and improving understanding of regulator
56 r data union and intersection, and candidate gene selection based on evidence in multiple datasets or
57 e test error rates to models based on single gene selection, but are more sparse as well as more stab
58 ally, scPNMF modifies the PNMF algorithm for gene selection by changing the initialization and adding
59 R5 interaction provides plasticity in target gene selection by MYC and speculate on the biochemical a
60 for network construction, module detection, gene selection, calculations of topological properties,
63 clude the dearth of proven selectable marker gene-selection combinations and tissue culture methods f
64 neuroligin, in addition to mRNA splicing and gene selection, contributes to the specificity of the ne
67 ms developed for single-cell RNA-seq adopted gene selection, dimension reduction or imputation to add
68 downstream analytical tasks such as variable gene selection, dimensional reduction, and differential
69 The mechanisms that regulate variable (V) gene selection during the development of the mouse IgH r
70 tes erroneous subdivisions, increases marker-gene selection efficacy, and efficiently scales to milli
71 in both the BM and spleen, suggesting that V-gene selection events correlate with CD23 expression in
73 hlighting the importance of stable reference gene selection for accurate expression normalization and
75 y, PCA projection facilitated discriminatory gene selection for different tissues and identified tiss
76 t the Affymetrix software and to rationalize gene selection for experimental designs involving limite
78 ds of genes and the small number of samples, gene selection has emerged as an important research prob
82 ep algorithm, Iterative Clustering and Guide-gene Selection (ICGS), which applies intra-gene correlat
83 iscuss the implication of this Zipf's law on gene selection in a microarray data analysis, as well as
86 shows that epithelioids recapitulate mutant gene selection in aging human esophagus and identifies a
87 Cancer Portal, a comprehensive catalogue of gene selection in cancer based purely on the biochemical
89 -mRNA sampling on gene expression and marker gene selection in single-cell and single-nucleus RNA-seq
91 A new cancer portal quantifies and presents gene selection in tumor over the entire human coding gen
93 e of phylogenetic variables including marker gene selection, inference methods, corrections for rate
94 a general framework to incorporate feature (gene) selection into pattern recognition in the process
95 It is yet unclear to what extent Hox target gene selection is dependent upon other regulatory factor
99 vector machines both in the settings when no gene selection is performed and when several popular gen
102 stering has been applied within our proposed gene selection method to satisfy both incorporated views
106 oduce sc-REnF [robust entropy based feature (gene) selection method], aiming to leverage the advantag
112 that scPNMF outperforms the state-of-the-art gene selection methods on diverse scRNA-seq datasets.
113 cross-platform comparisons and the impact of gene selection methods on the reproducibility of profili
114 rithm is more accurate than state-of-the-art gene selection methods that are particularly developed t
115 ms for multicategory classification, several gene selection methods, multiple ensemble classifier met
117 We apply POS, along-with four widely used gene selection methods, to several benchmark gene expres
120 situ horizontal gene transfer of resistance genes; selection of pre-existing resistance; and immigra
124 d with classification models based on single gene selections, our rules are stable in the sense that
125 sed on gene expression profiles suggest that gene selection plays a key role in improving the classif
126 However, the genes selected from one binary gene selection problem may reduce the classification per
127 FE (called MSVM-RFE) to solve the multiclass gene selection problem, based on different frameworks of
130 multivariate rank-distance correlation-based gene selection procedure (MrDcGene) to LUAD multi-omics
132 Very little attention has been given to gene selection procedures based on intergene correlation
133 ion methods, 10 reference datasets, 5 marker gene selection procedures, 5 data normalizations and 2 t
137 -based correlation information (iTwiner) for gene selection produced the best classification results
138 reveals the molecular basis of unique target gene selection/recognition, DNA binding cooperativity, a
139 hetic datasets, we find that anti-correlated gene selection reduces or eliminates erroneous subdivisi
140 ensitivity, reproducibility and stability of gene selection/sample classification to the choice of pa
141 everaging the structure of gene networks for gene selection, so that the relationship information bet
143 The method integrates information-theoretic gene selection, spatially weighted likelihood modeling,
144 a robust statistical approach for reference gene selection, stable genes selected from RNA-Seq data
145 taneously considering all classes during the gene selection stages, our proposed extensions identify
153 tion algorithms which used simple univariate gene selection strategy and constructed simple classific
154 l strategy, we propose a hierarchical marker gene selection strategy that groups similar cell cluster
155 his, we developed an effective computational gene selection strategy that represents public data abou
156 e Cross-Magnitude-Altitude Score (Cross-MAS) gene selection strategy, which integrates results across
157 odeling, supervised/unsupervised informative gene selection, supervised/unsupervised data visualizati
158 O was applied to a high-dimensional leukemia gene selection task, where it identified ultra-compact s
160 e gpsFISH, a computational method performing gene selection through optimizing detection of known cel
161 lts on chromosome 2q to prioritize candidate-gene selection, thus identifying SERPINE2 as a positiona
162 t direct Myc's recruitment to DNA and target gene selection to elicit specific cellular functions hav
163 n gene expression analysis is to improve hub gene selection to enrich for biological relevance or imp
164 Various computational models rely on random gene selection to infer such networks from microarray da
165 gnificant results in the current experiment, gene selection using an a priori hypothesis (neurodevelo
168 hat for datasets with large sample size, the gene-selection via the Wilcoxon rank sum test (a non-par
170 nd human microarray data to inform candidate-gene selection, we observed significant family-based ass
172 verall reliable performance in single marker gene selection, with COSG showing commendable speed and