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    Big Data in Omics and Imaging, Two Volume Set

    Big Data in Omics and Imaging, Two Volume Set by Xiong, Momiao;

    Series: Chapman & Hall/CRC Computational Biology Series;

      • GET 20% OFF

      • The discount is only available for 'Alert of Favourite Topics' newsletter recipients.
      • Publisher's listprice GBP 280.00
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        126 420 Ft (120 400 Ft + 5% VAT)
      • Discount 20% (cc. 25 284 Ft off)
      • Discounted price 101 136 Ft (96 320 Ft + 5% VAT)
      • Discount is valid until: 30 June 2026

    113 778 Ft

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    Availability

    Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
    Not in stock at Prospero.

    Why don't you give exact delivery time?

    Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.

    Short description:

    Introduces currently developed statistical methods and software for big genomic and epigenomic data analysis with real-world examples and case studies.

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    Long description:

    FEATURES


    Bridges the gap between the traditional statistical methods and computational tools for small genetic and epigenetic data analysis and the modern advanced statistical methods for big data


    Provides tools for high dimensional data reduction


    Discusses searching algorithms for model and variable selection including randomization algorithms, Proximal methods and matrix subset selection


    Provides real-world examples and case studies


    Will have an accompanying website with R code




    Provides a natural extension and companion volume to Big Data in Omic and Imaging: Association Analysis, but can be read independently.





    Introduce causal inference theory to genomic, epigenomic and imaging data analysis





    Develop novel statistics for genome-wide causation studies and epigenome-wide causation studies.





    Bridge the gap between the traditional association analysis and modern causation analysis





    Use combinatorial optimization methods and various causal models as a general framework for inferring multilevel omic and image causal networks





    Present statistical methods and computational algorithms for searching causal paths from genetic variant to disease





    Develop causal machine learning methods integrating causal inference and machine learning





    Develop statistics for testing significant difference in directed edge, path, and graphs, and for assessing causal relationships between two networks

    The book is designed for graduate students and researchers in genomics, bioinformatics, and data science. It represents the paradigm shift of genetic studies of complex diseases– from shallow to deep genomic analysis, from low-dimensional to high dimensional, multivariate to functional data analysis with next-generation sequencing (NGS) data, and from homogeneous populations to heterogeneous population and pedigree data analysis. Topics covered are: advanced matrix theory, convex optimization algorithms, generalized low rank models, functional data analysis techniques, deep learning principle and machine learning methods for modern association, interaction, pathway and network analysis of rare and common variants, biomarker identification, disease risk and drug response prediction.

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    Table of Contents:

    K25794:


    Mathematical Foundation.


    Linkage Disequilibrium.


    Association Studies for Qualitative Traits.


    Association Studies for Quantitative Traits.


    Multiple Phenotype Association Studies.


    K345128


    Preface


    Author


    1. Genotype–Phenotype Network Analysis


    2. Causal Analysis and Network Biology


    3. Wearable Computing and Genetic Analysis of Function-Valued Traits


    4. RNA-Seq Data Analysis


    5. Methylation Data Analysis


    6. Imaging and Genomics


    7. From Association Analysis to Integrated Causal Inference


    References


    Index

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