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[null,"1.","Record Nr.",null,"UNISA996503551803316"]
[null,null,"Titolo",null,"Handbook of statistical bioinformatics / / Henry Horng-Shing Lu [and three others]"]
[null,null,"Pubbl/distr/stampa",null,"Berlin : , : Springer, , [2022]"]
[{"$nulls":4},"©2022"]
[null,null,"ISBN",null,"3-662-65902-6"]
[null,null,"Edizione",null,"[2nd ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (406 pages)"]
[null,null,"Collana",null,"Springer Handbooks of Computational Statistics"]
[null,null,"Disciplina",null,"570.285"]
[null,null,"Soggetti",null,"Bioinformatics - Statistical methods"]
[{"$nulls":4},"Bioinformatics"]
[{"$nulls":4},"Bioinformàtica"]
[{"$nulls":4},"Biologia computacional"]
[{"$nulls":4},"Informàtica mèdica"]
[{"$nulls":4},"Estadística matemàtica"]
[{"$nulls":4},"Llibres electrònics"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,"Nota di contenuto",null,"Intro -- Preface -- Contents -- Part I Single-Cell Analysis -- Computational and Statistical Methods for Single-Cell RNA Sequencing Data -- 1 Introduction -- 2 Data Preprocessing -- 2.1 Reads Mapping -- 2.2 Cell Barcodes Demultiplexing -- 2.3 UMI Collapsing -- 2.4 Cell Barcodes Selection -- 2.5 Summary -- 3 Data Normalization and Visualization -- 3.1 Background -- 3.2 Global Scaling Normalization for UMI Data -- 3.3 Probabilistic Model-Based Normalization for UMI Data -- 3.4 Dimension Reduction and Cell Clustering -- 4 Dropout Imputation -- 4.1 Background -- 4.2 Cell-Cell Similarity-Based Imputation -- 4.3 Gene-Gene Similarity-Based Imputation -- 4.4 Gene-Gene and Cell-Cell Similarity-Based Imputation -- 4.5 Deep Neural Network-Based Imputation -- 4.6 G2S3 -- 4.7 Methods Evaluation and Comparison -- 5 Differential Expression Analysis -- 5.1 Background -- 5.2 DE Methods Ignoring Subject Effects -- 5.3 DE Methods Considering Subject Effects -- 5.4 iDESC -- 5.5 DE Methods Evaluation and Comparison -- 5.5.1 Type I Error Comparison -- 5.5.2 Statistical Power Comparison -- 6 Concluding Remarks -- References -- Pre-processing, Dimension Reduction, and Clustering for Single-Cell RNA-seq Data -- 1 Introduction -- 2 Pre-processing of scRNA-seq "]
[{"$nulls":4},"Data -- 2.1 Removal of Batch Effects -- 2.2 Quality Control and Feature Selection -- 3 Dimension Reduction and Clustering -- 3.1 Dimension Reduction -- 3.2 Clustering -- 4 Conclusion -- References -- Integrative Analyses of Single-Cell Multi-Omics Data: A Review from a Statistical Perspective -- 1 Multi-Omics Data Profiled on Different Cells -- 2 Multi-Omics Data Profiled on the Same Single Cells -- 3 Challenges and Future Perspectives -- References -- Approaches to Marker Gene Identification from Single-Cell RNA-Sequencing Data -- 1 Introduction."]
[{"$nulls":4},"2 Marker Gene Selection Relies on Identifying Differentially Expressed Genes -- 3 Methods for Marker Gene Selection -- 3.1 Highest Expressed, Highest Variable -- 4 Supervised Methods -- 4.1 COMET -- 4.2 scGeneFit -- 5 Unsupervised Methods -- 5.1 Seurat -- 5.2 SC3 -- 5.3 SCMarker -- 5.4 scTIM -- 5.5 RankCorr -- 6 Discussion -- References -- Model-Based Clustering of Single-Cell Omics Data -- 1 Introduction -- 2 Single-Cell Transcriptomic Data Clustering -- 2.1 Single-Cell Transcriptomic Data Structure -- 2.2 DIMM-SC -- 2.3 Real Data Example -- 3 Population-Scale Single-Cell Transcriptomic Data Clustering -- 3.1 Population-Scale Single-Cell Transcriptomic Data Structure -- 3.2 BAMM-SC -- 3.3 Real Data Example -- 4 Single-Cell Multi-omics Data Clustering -- 4.1 CITE-seq Data Structure -- 4.2 BREM-SC -- 4.3 Real Data Example -- 5 Concluding Remarks -- References -- Deep Learning Methods for Single-Cell Omics Data -- 1 Introduction -- 2 Factor-Model-Based Deep Learning Approaches -- 2.1 Regularization and Priors on the Latent Factors -- 2.1.1 Gaussian Prior and Variational Inference -- 2.1.2 Adjust for Batch Effects and Confounding Covariates: Identifiability -- 2.1.3 Adjust for Batch Effects and Confounding Covariates: Implementation -- 2.1.4 Model Cell Population Structure in the Latent Space -- 2.2 Distributional Assumptions on Observed Data -- 2.2.1 Model Observed Data from scRNA-seq -- 2.2.2 Model Observed Data from scATAC-seq -- 2.2.3 Model Observed Data from Single-Cell Multiomics Technologies -- 2.3 Post-training Statistical Analyses -- 2.3.1 Denoising -- 2.3.2 Visualization, Clustering, and Trajectory Analysis -- 2.3.3 Prediction -- 3 Deep Learning Methods for Dimension Reduction -- 3.1 Construct the Loss Function -- 3.2 Extra Penalties and Regularization -- 4 Discussion -- References -- Part II Network Analysis."]
[{"$nulls":4},"Probabilistic Graphical Models for Gene Regulatory Networks -- 1 Introduction -- 2 Probabilistic Graphical Models -- 2.1 Graphical Model Basics -- 2.2 Markov Networks -- 2.3 Bayesian Networks -- 3 Classic Graphical Models for Reconstructing GRNs -- 3.1 Frequentist Approach -- 3.2 Bayesian Approach -- 3.3 Graphical Models Incorporating Prior Knowledge -- 4 Testing in Graphical Models -- 4.1 Parametric Test -- 4.2 Non-parametric Test for Global Graph Structure -- 5 Conclusion -- References -- Additive Conditional Independence for Large and Complex Biological Structures -- 1 Additive Conditional Independence (ACI) -- 1.1 Additive Reproducing Kernel Hilbert Spaces and Relevant Linear Operators -- 2 Variable Selection via ACI -- 2.1 Nonparametric Variable Selection -- 2.2 Penalized Least-Square Estimation with RKHS Operators -- 2.3 Matrix Representation of Operators and Algorithm -- 2.4 Data Example -- 3 Graphical Modeling Through ACI -- 3.1 Nonparametric Graphical Models -- 3.2 The Additive Conditional Covariance and Partial Correlation Operators -- 3.3 Operator-Level Estimation and the Algorithm -- 3.4 Data Examples -- References -- Integration of Boolean and Bayesian Networks -- 1 Introduction -- 2 Methods -- 2.1 s-p-scores Associated with Networks, SPAN -- 2.2 Network Learning -- 3 Results -- 3.1 An Example -- 3.2 Real Example -- 3.3 Complex Example -- 4 Discussion -- References -- "]
[{"$nulls":4},"Computational Methods for Identifying MicroRNA-Gene Regulatory Modules -- 1 Introduction -- 2 Identifying MiRNA-Gene Modules by Integrating Heterogeneous Data Sources -- 2.1 Bipartite Graph-Based Methods -- 2.2 Nonnegative Matrix Factorization Methods -- 2.3 Statistical Modeling Approaches -- 3 Evaluating the Performance of MiRNA-Gene Module Identification Methods -- 4 Discussion -- 5 Conclusions -- References -- Causal Inference in Biostatistics -- 1 Introduction."]
[{"$nulls":4},"1.1 Causation and Association -- 1.2 Two Conceptual Frameworks: Causal Effect and Causal Discovery -- 2 Causal Effect -- 2.1 Approaches to Causal Inference -- 2.2 Randomized Clinical Trials -- 2.2.1 Perfect Randomized Trials -- 2.2.2 Randomized Trials with Missing Data -- 2.2.3 Randomized Trials with Post-treatment Variables -- 2.3 Observational Studies -- 2.3.1 Unconfounded Treatment Assignment Conditional on Measured Covariates -- 2.3.2 Unmeasured Cofounding -- 3 Some Current Research Topics -- 3.1 Heterogenous Treatment Effect and Precision Medicine -- 3.2 Integrating Data from Randomized Controlled Trials and Observational Studies -- 3.3 Multiple Treatments -- 4 Software Appendix -- References -- Bayesian Balance Mediation Analysis in Microbiome Studies -- 1 Introduction -- 2 Bayesian Balance Mediation Model -- 2.1 Bayesian Balance Mediation Model with a Binary Treatment -- 2.2 Direct and Mediation Effect and Estimation Based on Predictive Posterior Distribution -- 3 MCMC Sampling -- 3.1 MCMC Sampling -- 3.2 Conditional Distributions -- 4 Applications to Real Data -- 4.1 Mediation Analysis at the Phylum Level -- 4.2 Analysis at the Order Level -- 5 Simulation Studies -- 5.1 Data Generation -- 5.2 Simulation Result -- 6 Discussion -- References -- Part III Systems Biology -- Identifying Genetic Loci Associated with Complex Trait Variability -- 1 Introduction -- 2 The Concept of vQTL -- 3 Statistical Methods for vQTL Mapping -- 3.1 Classical Nonparametric Tests -- 3.2 Regression-Based Methods -- 3.3 Two-Stage Methods -- 3.4 Quantile Integral Linear Model (QUAIL) -- 3.5 Dispersion Effects -- 4 Applications of vQTL -- 4.1 Examples of vQTL -- 4.2 Screening vQTL for Candidate Loci Involved in GxE Interaction -- 4.3 Variance Polygenic Score -- 4.4 Other Applications and Future Directions -- References."]
[{"$nulls":4},"Cell Type-Specific Analysis for High-throughput Data -- 1 Introduction -- 2 Cell Type Composition Estimation -- 3 Cell Type-Specific Differential Analysis -- 4 Step-by-step Tutorial -- References -- Recent Development of Computational Methods in the Field of Epitranscriptomics -- 1 Introduction -- 2 MeRIP-seq and Other Technologies for RNA Modification Profiling -- 3 Methods to Analyze MeRIP-seq Data -- 3.1 Count-Based Methods for Simple Study Designs -- 3.2 Methods Compatible with Confounding Factors -- 3.3 A Guide for RNA Differential Methylation Analysis Using RADAR -- 4 Web Resources on m6A Epitranscriptome -- 4.1 Web Servers with m6A Site Prediction -- 4.2 m6A Epitranscriptome Database -- 5 Discussion -- References -- Estimation of Tumor Immune Signatures from Transcriptomics Data -- 1 Introduction -- 2 Regression-Based Deconvolution Algorithms -- 2.1 Linear Least Squares Regression -- 2.2 Support Vector Regression -- 2.3 Other Deconvolution Methods -- 3 Gene Set Enrichment-Based Methods and Other Gene-Based Algorithms -- 3.1 Gene Set Enrichment Analysis (GSEA) -- 3.2 Single-Sample GSEA (ssGSEA) -- 4 Benchmark Studies -- 5 Discussions -- References -- Cross-Linking Mass Spectrometry Data Analysis -- 1 Introduction -- 1.1 Peptide Identification Based on Mass Spectrometry -- 1.2 Cross-Linked Peptides Identification -- 1.2.1 Cross-Linker Selection -- 1.2.2 Chemical Reaction -- 1.2.3 Enzyme Digestion -- "]
[{"$nulls":4},"1.2.4 Enrichment of Cross-Linked Peptides -- 1.2.5 LC-MS and MS2 Acquisition -- 1.2.6 Data Interpretation -- 1.2.7 Quality Control -- 1.2.8 Downstream Applications -- 2 Non-cleavable Cross-Linking Methods -- 3 Cleavable Cross-Linking Methods -- 4 Time-Complexity Comparison Between Non-cleavable Methods and Cleavable Methods -- 5 False Discovery Rate in CL-MS -- 5.1 Target-Decoy Approach in Linear Peptides Identification."]
[{"$nulls":4},"5.2 TDA in Cross-Linked Peptides Identification."]