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| 21. Short Protocols in Molecular Biology (Short Protocols in Molecular Biology) | |
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| 22. Beginning Perl for Bioinformatics by James Tisdall | |
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Amazon.com Departing from O'Reilly's earlier monograph Developing Bioinformatic Computer Skills, Tisdall's text is organized aggressively along didactic lines. Nearly all of the 13 chapters begin with twin bullet lists of Perl programming tools and the bioinformatic methods that require them. Likewise, the chapters end with exercises. String concatenation is illustrated with gene splicing, and regular expressions are taught with gene transcription and motif searching. Tisdall emphasizes sequence examples throughout, leading up to an introduction to a Perl interface for the NIH GenBank biological database and the widely used BLAST sequence alignment tool. After a brief discussion of three-dimensional protein structure, he returns to sequence extraction and secondary structure prediction. Tisdall's goal is to boost the beginning programmer into a domain of self-learning. He imparts essential etiquette for the success of programming newbies: use the wealth or resources available, from user documentation to Web site surveys to FAQs to How-To's to news groups and finally to direct personal appeals for help from a senior colleague. A well-plugged-in bioinformatics Perl student will soon discover Bioperl, an open-source effort to bring research-grade bioinformatic tools to the Perl community. Bioperl is described briefly at the end of Tisdall's book and will reportedly be a forthcoming title of its own in the O'Reilly bioinformatics series. Although he introduces bioinformatics as an academic discipline, Tisdall treats it as a trade throughout his book. He indicates that open questions and computational hard problems exist, but does not describe what they are or how they are being tackled. Ultimately, Tisdall presents bioinformatics as another arrow in a bench scientist's quiver, very much like HPLC, 2D-PAGE, and the various spectroscopies. As odd as a "bioinformatics-as-tool" book may be to its research proponents, the reduction of bioinformatics to trade status both deflates and vindicates the years of research, as Tisdall's work attests. --Peter Leopold Reviews (16)
Superficially, this book isn't all that different from a lot of introductory Perl books: the Perl material starts out with an overview of the language, followed by a crash course on installing Perl, writing programs, and running them. From there, it goes on to introduce all the various language constructs, from variables to statements to subroutines, that any programmer is going to have to get comfortable with. Pretty run of the mill so far. Tisdall starts with two interesting assumptions, though: [1] that the reader may have never written a computer program before, and so needs to learn how to engineer a robust application that will do its job efficiently and well, and [2] that the reader wants to know how to write programs that can solve a series of biological problems, specifically in genetics and proteomics. As such, there is at least as much material about the problems that a biologist faces and the places she can go to get the data she needs as there is about the issues that a Perl programmer needs to be aware of. The author introduces the reader to the basics of DNA chemistry, the cellular processes that convert DNA to RNA and then proteins, and a little bit about how and why this is important to the biologist and what sorts of information would help a biologist's research. The main sources of public genetic data are noted, and the often confusing -- and huge -- datafiles that can be obtained from these sources are examined in detail. With the code he presents for solving these problems, Tisdall makes a point of not falling into the indecipherable-Perl trap: this is a useful language, well-suited to the essentially text-analysis problems that bioinformatics means, and he doesn't want to encourage the kind of dense, obscure, idiomatic coding style that has given Perl an undeservedly bad reputation. Some of Perl's more esoteric constructs are useful, and they show up when they're needed, but they're left out when they would only serve to confuse the reader. This is a good decision. Rather, the focus is on teaching readers how to solve biological problems with a carefully developed library of code that happens to leverage some of Perl's most useful properties. The result is pretty much a biologist's edition of Christiansen & Torkington's Perl Cookbook or Dave Cross' Data Munging With Perl. The author presents a series of issues that a working bioinformaticist might have to deal with daily -- parsing over BLAST, GenBank, and PDB files, finding relevant motifs in that parsed data, and preparing reports about all of it. If a bioinformaticist's job is to be able to report on interesting patterns from these various sources, then following the programming techniques that Tisdall explains in clear, easy-to-follow prose would be an excellent way to go about doing it. And when I say "programming techniques," note that I'm not specifically mentioning Perl. The code in this book is clear and organized, and all programs are carefully decomposed into logical subroutines that are then packaged up into a library file that each later sample program gets to draw from. Each new program typically contains a main section of a dozen lines of code or less, followed by no more than two or three new subroutines, along with calls to routines written earlier and called from the BeginPerlBioinfo.pm that is built up as the book progresses. Each sample is typically preceded by a description of what it's trying to accomplish and followed by a detaild description of how it was done, as well as suggestions of other ways that might have worked or not worked. This modular approach is fantastic -- too many Perl books seem to focus so heavily on the mechanics of getting short scripts to work that they lose sight of how to build up a suite of useful methods and, from those methods, to develop ever-more-sophisticated applications. It isn't quite object-oriented programming, but that's clearly where Tisdall is headed with these samples, and given a few more chapters he probably would have started formally wrapping some of this code into OO packages. If I have a complaint with the book, in fact, it's that Tisdall doesn't go any further: everything is good, but it ends too soon. Seemingly important topics such as OO programming, XML, graphics (charts & GUIs), CGI, and DBI are mentioned only in passing, under "further topics" in the last chapter. I also have a feeling that some of the biology was shorted, and the book barely touches upon the statistical analysis that probably is a critical aspect of the advanced bioinformaticist's toolbox. I can understand wanting to keep the length of a beginner's book relatively short, and this was probably the right decision, but it would have been nice to see some of the earlier sample problems revisited in these new contexts by, for example, formally making an OO library, showing a sample program that provided a web interface to some of the methods already written, or presenting code that presented results as XML or exchanged them with a database. But these are minor quibbles, and if the reader is comfortable with the material up to this point, she shouldn't have a hard time figuring out how to go a step further and do these things alone. It's a solid book, and one that should be able to get people learning Perl, genetics, or both up to speed and working on real world problems quickly.
Also, I do not like the fact that it uses "quick and dirty" Perl (no "use strict" pragma). While it might be less confusing to skip it at the very beginning, very soon students start to waste too much precious class time trying to locate bugs that would make the program not compile with "use strict" in the first place (e.g. mistyped variable names).
The consensus in the field seems to be that it's more productive (and certainly easier) to teach biologists how to program, rather than try to get programmers up to speed on the intracities of molecular biology. For similar reasons, Perl is a popular language to learn: it's easy to get off the ground and be productive with it, without requiring a heavy computer science background. (This, of course, has downsides as well...) Never one to miss out on a trend, I'm going to be teaching a course on Bioperl and advanced Perl programming, starting next fall, which means I'm doing a lot of reading in this topic area, trying to develop lectures and find good background reading material. One of the first books I grabbed was _Beginning Perl for Bioinformatics_, which has been sitting on my "to read" shelf since O'Reilly sent me a review copy in December of 2001. It's a typical O'Reilly "animal" book (the cover bears three tadpoles), which does a decent job of introducing the basic features of the Perl language, and it should enable a dedicated student to get to the point where she can produce small useful programs. However, I'm not completely happy about the book's organization, and I think the occasional "if you're not a biologist, here's some background" interjections could have been cut without hurting anything. The initial chapters in the book cover "meta" information, such as theoretical limits to computation, installing (or finding) the Perl interpreter on your computer, picking a text editor, and locating on-line documentation. Some general programming theory stuff is covered as well -- the code-run-debug cycle, top-down versus bottom-up design, the use of pseudocode. There's also some biology background, but it's very introductory level stuff -- DNA has four bases, proteins are made of 20 amino acids, and so on. In chapter four, the book begins to get into actual Perl, with some coverage of string manipulation. Examples deal with simulating the transcription of DNA into RNA. Chapters five and six continue to flesh out the language, covering loops, basic file I/O, and subroutines. Chapter seven introduces the rand() function, in the context of simulating mutations in DNA. Subsequent chapters introduce the hash data type (using a RNA->protein translation simulation), regular expressions (as a way to store the recognition patterns of restriction endonucleases), and parsing database flat files and BLAST program output. I'm clearly out of the target audience of the book, as I already have a strong working knowledge of Perl. Perhaps that's why I found the order that concepts were presented in to be a bit strange -- for example, hashes, which are a fundamental data type, aren't introduced until halfway through the book, and regular expressions (one of the key features of Perl) first appear even later. As I said above, I also found the biological background sections to be more distracting than anything, but I've also got a strong biology background, so perhaps I'm off base here too. That said, I think a person with a CS background would be better served with a copy of _Learning Perl_ and an introductory molecular biology text than with this particular book. One of the things I did enjoy about the book were the frequent coding examples, all of which presented realistic computational biology sorts of problems and then demonstrated how to solve them. I'm sure that when I get around to writing lectures, I'll be leafing through this book looking for problems I can use in class. Overall, recommended for biologists without programming experience who would like to get started using Perl for simple programming. Not recommended for people with computer science backgrounds looking to get into bioinformatics.
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| 23. Genes VII by Benjamin Lewin | |
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Book Description THE MOST SIGNIFICANT REORGANIZATION TO DATE The power of direct analysis of the genome has made a significant difference in the approach of GENES VII. In a departure from previous editions, which started with a traditional analysis of formal genetics, the new edition begins with the molecular properties of the gene itself. The text is now reorganized to begin with the concept of genes as a segment of DNA coding for protein, and then proceeds directly to the characterization of the genome in terms of its content of genes. INTEGRATED APPROACH GENES VII first explains the structure and function of the gene as a means to revealing the operation of the genome as a whole, and offers an integrated approach to prokaryotes and eukaryotes. The gene is considered from all aspects, including: * Basic forms * The numbers and relationships among genes in a genome * Their packaging into chromosomes * The process of gene expression from transcription through translation * The reproduction and safeguarding of the gene structure * Aspects of the overall circuitry through which genotype determines phenotype STREAMLINED, FULL-COLOR DESIGN GENES VII has been considerably restructured and reorganized to highlight the latest research and technology. It contains more that 800 full color illustrations that are extremely useful in teaching the key concepts presented in the book. GENES VII CONTAINS NEW, GROUNDBREAKING INFORMATION ON: * New technologies that count and compare expressed genes * Accessory proteins (chaperones) * The role of the proteasome * Licensing * Reverse translocation * Connections between repair and recombination systems and human diseases * Connections between the structure of chromosomal material and control of gene expression in eukaryotes * The process of X chromosome inactivation * Imprinting * Control of gene expression by epigenetic changes * The enzymatic activities that control chromatin structure and affect the regulatory process * Archeael enzymes * The mechanism of RNA editing in lower eukaryotes * The role of RAG genes * Interactions within and between pathways * The use of protein degradation to control passage through the cell cycle * Programmed cell death * Telomerase and its role in carcinogenesis. And much more! Reviews (21)
I am in my second year of teaching from this book and I find it very frustrating. Lewin's writing style is unclear, difficult and distracting. Tangential ideas and subjects appear out of nowhere in the middle of chapters for no logical reason. As I write this, I should be preparing my lecture for Chapter 26 (Signal transduction). Why does this chapter start with a discussion of transporters? Later parts contain sentences that are almost unreadable and way too much detail about the alphabet soup of different kinases. Although it is much better than some earlier editions, Genes VII still contains a variety of major and minor errors, including serious problems in explaining how lagging strand DNA synthesis is coordinated in the replication fork - several experts tell me that the model in figure 13.16 is simply wrong. The holoenyme does not lose one of its catalytic subunits with each cycle of Okazaki fragment synthesis. The clamp simply lets go and the clamp loader grabs the next fragment with a new clamp. I realized this semester that I had been ignoring the book and teaching what I knew from seminars. Even when the content they describe is basically correct, figures in Genes VII can be astonishingly bad. Homologous recombination is illustrated with DNA strands that are only color coded and where the 5' and 3' ends are not labeled (Chapter 14). Unlabeled spliceosomal proteins change their color codes in the middle of the pathway - transesterification to form the lariat also seems to change U2 into U1 (Figure 22.10). I am hoping that one of the newer competitors for Genes VII will prove to be a suitable replacement. I am examining Robert Weaver's Molecular Biology - I like what I've read so far - and should get a review copy of T.A. Brown's Genomes soon. ...Disclaimer - I have no financial interest in the success of any of these. All of them are available on Amazon. By the way, I do have a Ph.D. in Molecular Biology. I'm not an expert in all of the material covered by Genes VII, but I was trained in labs whose work is cited in Genes VII.
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| 24. Bioinformatics: Sequence and Genome Analysis by David W. Mount | |
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Book Description It is written for any biologist who wants to understand methods of sequence and structure analysis and how the necessary computer programs work Sequence alignment, structure prediction, phylogenetic and gene prediction, database searching, and genome analysis are clearly explained and amply illustrated Underlying algorithms and assumptions are clearly explained for the non-specialist Examples are presented in simple numerical terms rather than complex formulas and notation Theoretical underpinnings are linked to biological problems and their solutions Extensive tables provide descriptions and Web sources for a broad range of publicly available software Based on the author's extensive experience as a molecular geneticist and bioinformaticist at the University of Arizona, this is a uniquely educational book, ideal as a laboratory reference for investigators and also as teaching reference for graduate and undergraduate students studying this fast-changing discipline. Reviews (14)
I purchased this book a while ago. At that time, the book was really difficult to read. I thought that it is because I do not have enough knowledge to understand the material. So I stopped reading this book and studied bioinformatics by other means. After gaining enough knowledge in bioinformatics, I re-opened this book, and it is funny to find that I still have the same amount of difficulty in understanding what the author wrote about topics that I have already built good understanding. Reading this book will only deteriorate one's understanding. Several years ago, only just a few books were available on the market, so one needed to purchase this book. These days, there are lots of varieties to choose, and any choice is likely to be better than this book.
This book has a good coverage of FASTA and The programming techniques coverd are bare. Though I am yet to find a good book that deals only with On the whole this book helped me understand a lot If you are reading this review pls understand that I am Hope this helps Santy
So far, the best there is for a survey course - but for depth and accuracy in sequence analysis algorithms, go to Durbin et al or Gussfield. ... Read more | |
| 25. A Pharmacology Primer : Theory, Application and Methods by Terry, Ph.D. Kenakin, Terrence P. Kenakin | |
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| 26. Pcr (Basics: from Background to Bench) by M. J. McPherson, S. G. Møller, R. Beynon, C. Howe | |
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| 27. Fundamentals of Molecular Evolution by Dan Graur, Wen-Hsiung Li | |
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Book Description The authors explain evolutionary phenomena at the molecular level in a way that can be understood without much prerequisite knowledge of molecular biology, evolution, or mathematics. Both mathematical and intuitive explanations are provided, and examples that support and clarify the many theoretical arguments and methodological discussions are included. Reviews (3)
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| 28. Molecular Biotechnology: Principles and Applications of Recombinant DNA by Bernard R. Glick, Jack J. Pasternak | |
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| 29. Mobile DNA II | |
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| 30. Genomes by Terence A. Brown | |
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| 31. Bioinformatics and Functional Genomics by Jonathan Pevsner | |
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Book Description Reviews (3)
Now, for the book itself. It is easy to read and covers all aspects of bioinformatics from a sequence perspective (information retrieval, BLAST, gene expression and microarrays, proteomics and protein bioinformatics, genomes and disease). The coverage of databases and URLs is thourough and the text is easy to read, yet useful. The book is comprehensive with one area seemingly missing -- it would have been useful to include a chapter on systems biology and/or cellular modeling and the tools available (i.e. E-Cell). The book is especially useful to a researcher who is trying to explore all aspects of a particular gene, protein, disease, or pathway using bioinformatics tools. The book is in stark contrast to the other Pevser (that is Pevzner) who wrote a bioinformatics book that surveyed algorithm theory underlying bioinformatics. This book is also useful for less technical professionals in industry -- the managers, lawyers and venture capitalists that pervade the biotech landscape all need to communicate effectively and they can surely learn that here, provided they have some background in cell biology first.
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| 32. Molecular Cloning: A Laboratory Manual (3-Volume Set) by Joseph Sambrook, David W. Russell, Joe Sambrook | |
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Book Description In this new edition, authors Joe Sambrook and David Russell have completely updated the book, revising every protocol and adding a mass of new material, to broaden its scope and maintain its unbeatable value for studies in genetics, molecular cell biology, developmental biology, microbiology, neuroscience, and immunology. Handsomely redesigned and presented in new bindings of proven durability, this three-volume work is essential for everyone using todays biomolecular techniques. The opening chapters describe essential techniques, some well-established, some new, that are used every day in the best laboratories for isolating, analyzing and cloning DNA molecules, both large and small. These are followed by chapters on cDNA cloning and exon trapping, amplification of DNA, generation and use of nucleic acid probes, mutagenesis, and DNA sequencing. The concluding chapters deal with methods to screen expression libraries, express cloned genes in both prokaryotes and eukaryotic cells, analyze transcripts and proteins, and detect protein-protein interactions. The Appendix is a compendium of reagents, vectors, media, technical suppliers, kits, electronic resources and other essential information. As in earlier editions, this is the only manual that explains how to achieve success in cloning and provides a wealth of information about why techniques work, how they were first developed, and how they have evolved. Reviews (13)
At the beginning of each chapter, the authors give an introduction to the protocols and this is of an enormous help to those readers with only rudimentary acquaintance with the laboratory procedures. Typically, this introduction contains an historical summary of the procedures as they were developed or discovered. One can only marvel at the ingenuity of the discoverers of these techniques. These introductions are fairly straightforward to read, even for those that are not experts in biochemistry. At the end of each chapter, the authors include an "information panel" that gives a more in-depth view of the biochemistry or genetics behind the procedures. These are summaries and are highly specialized, and are again meant for experienced readers. A very lengthy list of references is also included at the end of each chapter. Becuase of the size of this collection, space here does not permit a detailed review, so I will list some of the areas that I thought were particularly interesting or well-written (these coming from the introduction or the information panels only): 1. The DNA synthesis at the colE1 replicon and the interaction between RNAI and RNAII. 2. The discussion of electroporation and the physics behind this technique to introduce DNA into eukaryotic cells. 3. The discussion on the discovery of bacteriophage lambda. 4. The discussion (with diagram), of the assembly pathway of bacteriophage lambda. 5. The summary of the early analysis of DNA using electrophoresis and the different pulsed-field configurations used. 6. The anecdote on the discovery of the polymerase chain reaction. 7. The short discussion on computer-assisted design of oligonucleotide primers. 8. The discussion of oligonucleotide synthesis. 9. The flowchart detailing the preparing and screening of a cDNA library. 10. The history of the development of the methods to synthesize and clone cDNAs. 11. The detailed discussion of the molecular cloning of double-stranded cDNA. 12. The discussion on the methods to validate clones of cDNA. 13. The discussion on magnetic beads for affinity purification. 14. The discussion on the history of DNA sequencing and the different techniques to accomplish it, particularly the information panel on automated DNA sequencing. 15. The discussion of the different types of mutagenesis and the different methods for accomplishing it. 18. The fascinating discussion of how to introduce cloned genes into mammalian cells. 19. The discussion on the steps involved in DNA footprinting. 20 The discussion on green flourescent protein and its use as a fusion tag. 21. The discussion on the use of surface plasmon resonance spectroscopy.
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| 33. iGenetics : A Molecular Approach (2nd Edition) by Peter J. Russell | |
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Book Description iGenetics: A Molecular Approach reflects the dynamic nature of modern genetics by emphasizing an experimental, inquiry-based approach with a solid treatment of many research experiments. Genetics: An Introduction, DNA: The Genetic Material, DNA Replication, Gene Control of Proteins, Gene Expression: Transcription, Gene Expression: Translation, DNA Mutation, DNA Repair, and Transposable Elements, Recombinant DNA Technology, Applications of Recombinant DNA Technology, Genomics, Mendelian Genetics, Chromosomal Basis of Inheritance,Extensions of Mendelian Genetic Principles, Quantitative Genetics, Gene Mapping in Eukaryotes, Advanced Gene Mapping in Eukaryotes, Variation in Chromosome Number and Structure, Genetic Analysis of Bacteria and Bacteriophages, Regulation Of Gene Expression In Bacteria And Bacteriophages, Regulation Of Gene Expression In Eukaryotes, Genetic Analysis Of Development, Genetics Of Cancer, Non-Mendelian Inheritance, Population Genetics, Molecular Evolution. For all readers interested in learning the central concepts of genetics. | |
| 34. Handbook of Proteolytic Enzymes, Two-Volume Set with CD-ROM | |
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| 35. Advances in Protein Chemistry, Volume 51: Linkage Thermodynamics of Macromolecular Interactions by Federic Richards | |
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| 36. Discovering Genomics, Proteomics, and Bioinformatics by A. Malcolm Campbell, Laurie J. Heyer | |
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Book Description Reviews (1)
Recommended to students: yes, together with classic works like Brown. Recommended to Central Library: yes. 1. The supplied CD-ROM is a nice teaching aid. Yet, it is difficult to "extract" pictures from it for teaching purposes. It would be much more useful if the pictures were individually supplied in standard high-quality graphic formats like TIFF, instead of PDF. The later is perfect for distributing text with pictures, but not to retrieve such pictures. Other publishers distribute the book artwork as individual TIFF files. That approach greatly enhances the book and boost sales. This is particularly useful for teachers. Actually, it is a must for us these days. Please, make sure that future versions of the CD-ROM or DVD-ROM are --as this one-- compatible with the open-source Unix-based Mac OS X platform. Thanks. 2. The associated web page "Instructor's Guide" 4. Math minutes are an excellent idea. 5. Boxes are welcome. Please, include more. 6. Also helpful are the boldface words on each chapter. Perhaps they could be also included in a keywords at the beginning of each chapter. 7. The index should be more comprehensive and should have all main entries in boldface. This is important to any index and very few books have it right. 8. The glossary is helpful. It should be more comprehensive, 9. The summaries and conclusions are great, yet should be expanded to include more relevant information. They should be like a "minichapter" an the end of each chapter or --better-- at the beginning. All partial summaries could be pooled into a larger summary that way. 10. Addendum sections could be included as separate notes or boxes. 11. The pronunciation tips for new words are also an excellent idea; mostly for non-English speakers. 12. The classified references are really useful. Well done. If they were commented or "annotated" they would be just perfect. 13. A list of abbreviations would be welcome. A list sorted by the full name would be very handy as well. 14. What about telomerase and aging? What about the fact that 15. It should be clearly indicated the organisms with genomes made of dsDNA, ssDNA, dsRNA and ssRNA. 16. Missing bioinformatics tools and step-by-step analysis of genes and mRNA (see next) and whole genomes. 17. It would be really helpful to explain clearly and analyze --even from a bioinformatics point of view-- the structure of genes, mRNA, CDS, introns, exons, promoters and terminators. It is not clear where do these elements start or end or how to recognize them. Diagrams and graphs would greatly help to explain these absolutely basic and fundamental concepts. In other words, imagine that you have cloned and sequenced a genomic gene as well as a full mRNA (cDNA). Now you want to publish your results and for that you do a comprehensive description of your gene (chromosome) and cDNA (mRNA). That is precisely the kind of information that is missing as a diagram and explanation. In this way, it should be indicated that you may encounter several ATG (or other) starting coding triplets in the mRNA, that if the 20 or so amino acid residues of the 5'-end of a peptide have a high percentage of hydrophobic residues, they are likely part of a leading peptide which would be further excised, that you may encounter several polyadenylation signals, etc. On the genome side, the promoter and terminator structures should be analyzed, as well as the intron-exon boundaries. 18. Likewise, it should be indicated the tools and current 19. Does not mention Lasergene package of DNAStar 21. Differential display methodologies are missing (as well as other methodologies of gene expression like subtractive hybridization). 22. Large-scale sequencing is missing. For instance, sequencing of single-molecules will allow the sequencing of whole chromosomes or genomes. 23. Missing tables comparing different genomes with full details 24. Reference to manufacturers is very useful. Please, include also links to web sites. Best if all manufacturers are included as an appendix. 25. All web sites (NCBI, etc) and web-based applications (BLAST, ORF Finder, etc) should be clearly indicted in an appendix. 26. It is not indicated that the PCR was in fact described with full details by Khorana et al 14 years before Mullis et al. 27. Please, include more drawings and pictures in the printed book and CD-ROM. 28. Suggestion: including chapters on eukaryotic-genomic DNA 29. Suggestion: including chapters on plant and animal transformation. 30. Suggestion: including drawing of Maxam-Gilbert sequencing method and Sanger method (Applied Biosystems electropherograms, 31. Prions, viroids and viruses could be also included. 32. A title index at the beginning of each chapter would be very 33. Bioinformatics could be significantly expanded. 34. QuickTime videos explaining some topics would be fantastic. 35. All in all, a great novel approach. Keep up the great work!
... Read more | |
| 37. DNA Microarrays and Gene Expression : From Experiments to Data Analysis and Modeling by Pierre Baldi, G. Wesley Hatfield, Wesley G. Hatfield | |
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| 38. Molecular Systematics by David M. Hillis, Craig Moritz, Barbara K. Mable | |
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our price: $82.95 (price subject to change: see help) Asin: 0878932828 Catlog: Book (1996-01-01) Publisher: Sinauer Associates Sales Rank: 256898 Average Customer Review: US | Canada | United Kingdom | Germany | France | Japan |
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Book Description Molecular Systematics includes chapters on sampling design, the collection and storage of tissues, each of the major molecular techniques, and intraspecific and phylogenetic analysis. The sampling chapters describe how to plan a study and how to collect, transport, and store the appropriate tissues for each study. The techniques chapters cover principles, assumptions, applications, limitations, and pr | |