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  • 1
    Online Resource
    Online Resource
    Bioinformatics tools for detection and clinical interpretation of genomic variations (2019)
    London : IntechOpen
    Details
    UID:
    b3kat_BV046304166
    Format: 1 Online-Ressource , Illustrationen
    ISBN: 9781789238006 , 9781838818449
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-1-78923-799-3
    Language: English
    DOI: 10.5772/intechopen.77443
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    Fulltext
    Fulltext
    HTW Berlin
    TH Wildau
  • 2
    Online Resource
    Online Resource
    Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations (2019)
    [Erscheinungsort nicht ermittelbar] : IntechOpen
    Details
    UID:
    gbv_1778478565
    Format: 1 Online-Ressource (100 p.)
    ISBN: 9781789238006 , 9781789237993 , 9781838818449
    Content: Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you
    Note: English
    Language: English
    URL: kostenfrei
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    Stabi Berlin
    UB Potsdam
  • 3
    Online Resource
    Online Resource
    Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / (2019)
    IntechOpen | London, United Kingdom :IntechOpen,
    Details
    UID:
    almafu_9959162985302883
    Format: 1 online resource (100 pages)
    ISBN: 1-83881-844-8 , 1-78923-800-5
    Content: Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you.
    Note: English
    Additional Edition: ISBN 1-78923-799-8
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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    Online Resource
    FU Berlin
    Charité
  • 4
    Online Resource
    Online Resource
    Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / (2019)
    IntechOpen | London, United Kingdom :IntechOpen,
    Details
    UID:
    almahu_9949281735102882
    Format: 1 online resource (100 pages)
    ISBN: 1-83881-844-8 , 1-78923-800-5
    Content: Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you.
    Note: English
    Additional Edition: ISBN 1-78923-799-8
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    HU Berlin
  • 5
    Online Resource
    Online Resource
    Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / (2019)
    IntechOpen | London, United Kingdom :IntechOpen,
    Details
    UID:
    edocfu_9959162985302883
    Format: 1 online resource (100 pages)
    ISBN: 1-83881-844-8 , 1-78923-800-5
    Content: Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you.
    Note: English
    Additional Edition: ISBN 1-78923-799-8
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    FU Berlin
  • 6
    Online Resource
    Online Resource
    Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / (2019)
    IntechOpen | London, United Kingdom :IntechOpen,
    Details
    UID:
    edoccha_9959162985302883
    Format: 1 online resource (100 pages)
    ISBN: 1-83881-844-8 , 1-78923-800-5
    Content: Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you.
    Note: English
    Additional Edition: ISBN 1-78923-799-8
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Charité
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