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"Genomic structural variants" was published by Humana Press in 2012 - New York, it has 386 pages and the language of the book is English.


“Genomic structural variants” Metadata:

  • Title: Genomic structural variants
  • Author:
  • Language: English
  • Number of Pages: 386
  • Publisher: Humana Press
  • Publish Date:
  • Publish Location: New York

“Genomic structural variants” Subjects and Themes:

Edition Specifications:

  • Pagination: xi, 386 p. :

Edition Identifiers:

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"Genomic structural variants" Table Of Contents:

  • 1- What have studies of genomic disorders taught us about our genome? -- Alexandra D. Simmons, Claudia M.B. Carvalho,and James R. Lupski
  • 2- Microdeletion and microduplication syndromes -- Lisenka E.L.M. Vissers and Paweł Stankiewicz
  • 3- Structural genomic variation in intellectual disability -- Rolph Pfundt and Joris A. Veltman
  • 4- Copy number variation and psychiatric disease risk -- Rebecca J. Levy ... [et al.]
  • 5- Detection and characterization of copy number variation in autism spectrum disorder -- Christian R. Marshall and Stephen W. Scherer -- Structural variation in subtelomeres / -- M. Katharine Rudd
  • 6- Array-based approaches in prenatal diagnosis -- Paul D. Brady ... [et al.]
  • 7- Structural variation and its effect on expression -- Louise Harewood, Evelyne Chaignat, and Alexandre Reymond
  • 8- Challenges of studying complex and dynamic regions of the human genome -- Edward J. Hollox
  • 9- Population genetic nature of copy number variation -- Per Sjödin and Mattias Jakobsson
  • 10- Detection and interpretation of genomic structural variation in mammals -- Ira M. Hall and Aaron R. Quinlan
  • 11- Structural genetic variation in the context of somatic mosaicism -- Jan P. Dumanski and Arkadiusz Piotrowski
  • 12- Online resources for genomic structural variation -- Tam P. Sneddon and Deanna M. Church
  • 13- Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data -- Laura Winchester and Jiannis Ragoussis
  • 14- Targeted screening and validation of copy number variations -- Shana Ceulemans, Karlijn van der Ven, and Jurgen Del-Favero
  • 15- High-resolution copy number profiling by array CGH using DNA isolated from formalin-fixed, paraffin-embedded tissues -- Hendrik F. van Essen and Bauke Ylstra
  • 16- Characterizing and interpreting genetic variation from personal genome sequencing -- Anna C.V. Johansson and Lars Feuk
  • 17- Massively parallel sequencing approaches for characterization of structural variation -- Daniel C. Koboldt ... [et al.].

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