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Comparative Genomics Volume 2 at Meripustak

Comparative Genomics Volume 2 by Nicholas H. Bergman , Humana Press Inc.

Books from same Author: Nicholas H. Bergman

Books from same Publisher: Humana Press Inc.

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  • General Information  
    Author(s)Nicholas H. Bergman
    PublisherHumana Press Inc.
    ISBN9781934115374
    Pages434
    BindingHardback
    LanguageEnglish
    Publish YearDecember 2007

    Description

    Humana Press Inc. Comparative Genomics Volume 2 by Nicholas H. Bergman

    This volume provides a collection of robust protocols for molecular biologists studying comparative genomics. Each chapter includes detailed instructions for using a particular tool or method and an introduction to the theory behind the technique. Given the tremendous increase in available biosequence data over the past ten years, this volume is timely, comprehensive, and novel._x000D_ _x000D_ Comparative Genomics-Volume II_x000D_ _x000D_ Table of Contents_x000D_ _x000D_ Section V-Comparative Analysis of Domain and Protein Families_x000D_ _x000D_ 1. Computational Prediction of Domain Interactions_x000D_ Philipp Pagel, Normann Strack, Matthias Oesterheld, Volker Stumpflen,_x000D_ and Dmitrij Frishman_x000D_ 2. DomainTeam: Synteny of domains is a new approach in comparative_x000D_ genomics_x000D_ Sophie Pasek_x000D_ 3. Inference of gene function based on gene fusion events: the Rosetta_x000D_ Stone method_x000D_ Karsten Suhre_x000D_ 4. Pfam: A domain-centric method for analyzing proteins and proteomes_x000D_ Jaina Mistry and Robert Finn_x000D_ 5. InterPro and InterProScan-Tools for Protein Sequence Classification_x000D_ and Comparison_x000D_ Nicola Mulder and Rolf Apweiler_x000D_ 6. Gene Annotation and Pathway Mapping in KEGG_x000D_ Kiyoko F. Aoki-Kinoshita and Minoru Kanehisa_x000D_ _x000D_ _x000D_ Section VI-Orthologs, Synteny, and Genome Evolution_x000D_ _x000D_ 7. Ortholog Detection using the Smallest Distance Algorithm_x000D_ Dennis P. Wall and Todd DeLuca_x000D_ 8. Finding Conserved Gene Order Across Multiple Genomes_x000D_ Giulio Pavesi and Graziano Pesole_x000D_ 9. Analysis of Genome Rearrangement by Block-Interchanges_x000D_ Chin Lung Lu, Ying Chih Lin, Yen Lin Huang, and Chuan Yi Tang_x000D_ 10. Analyzing Patterns of microbial evolution using the Mauve Genome_x000D_ Alignment System_x000D_ Aaron E. Darling, Todd J. Treangen, Xavier Messeguer, and Nicole T._x000D_ Perna_x000D_ 11. Visualization of syntenic relationships with SynBrowse_x000D_ Volker Brendel, Stefan Kurtz, and Xiaohang Pan_x000D_ 12. GECKO and GHOSTFAM: Rigorous and Efficient Gene Cluster Detection_x000D_ in Prokaryotic Genomes_x000D_ Thomas Schmidt and Jens Stoye_x000D_ _x000D_ _x000D_ Section VII-Experimental Analysis of Whole Genomes-Analysis of Copy_x000D_ Number and Sequence Polymorphisms_x000D_ _x000D_ 13. Genome-wide copy number analysis on GeneChip platform using CNAG_x000D_ 2.0 software_x000D_ Seishi Ogawa, Yasuhito Nanya, and Go Yamamoto_x000D_ 14. Oligonucleotide array comparative genomic hybridization_x000D_ Paul van den IJssel and Bauke Ylstra_x000D_ 15. StudyingBacterial Genome Dynamics Using Microarray-Based_x000D_ Comparative Genomic Hybridization_x000D_ Eduardo N. Taboada, Christian C. Luebbert, and John H.E. Nash_x000D_ 16. CGH analysis using the CGHAnalyzer_x000D_ Joel Greshock_x000D_ 17. Microarray-based Approach for Genome-Wide Survey of Nucleotide_x000D_ Polymorphisms_x000D_ Brian W. Brunelle and Tracy L. Nicholson_x000D_ 18. High-Throughput Genotyping of Single Nucleotide Polymorphisms with_x000D_ High Sensitivity_x000D_ Honghua Li, Hui-Yun Wang, Xiangfeng Cui, Minjie Luo, Guohong Hu,_x000D_ Danielle M. Greenawalt, Irina V. Tereshchenko, James Y. Li, Yi Chu, and_x000D_ Richeng Gao_x000D_ 19. Single nucleotide polymorphism (SNP) mapping array assay_x000D_ Xiaofeng Zhou and David T. W. Wong_x000D_ 20. Molecular Inversion Probe Assays_x000D_ Farnaz Absalan and Mostafa Ronaghi_x000D_ 21. novoSNP: variant detection and sequence annotation in resequencing_x000D_ projects_x000D_ Peter De Rijk and Jurgen Del-Favero_x000D_ 22. Rapid Identification of Single Nucleotide Substitutions Using_x000D_ SeqDoc_x000D_ Mark L. Crowe_x000D_ 23. SNPHunter: A Versatile Web-Based Tool for Acquiring and Managing_x000D_ Single Nucleotide Polymorphisms_x000D_ Tianhua Niu_x000D_ 24. Identification of Disease Genes: An Example-driven Web-based_x000D_ Tutorial_x000D_ Medha Bhagwat_x000D_ 25. Variable number tandem repeat typing of bacteria_x000D_ Siamak P. Yazdankhah and Bjorn-Arne Lindstedt_x000D_ 26. Fluorescent amplified fragment length polymorphism (FAFLP)_x000D_ genotyping of bacterial species_x000D_ Meeta Desai_x000D_ 27. FLP-mapping: A universal, cost-effective, and automatable method_x000D_ for gene mapping_x000D_ Knud Nairz, Peder Zipperlen, and Manuel Schneider_x000D_



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