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Paperback Sequence Analysis in a Nutshell: A Guide to Tools: A Guide to Common Tools and Databases Book

ISBN: 059600494X

ISBN13: 9780596004941

Sequence Analysis in a Nutshell: A Guide to Tools: A Guide to Common Tools and Databases

Gene sequence data is the most abundant type of data available, and if you're interested in analyzing it, you'll find a wealth of computational methods and tools to help you. In fact, finding the data is not the challenge at all; rather it is dealing with the plethora of flat file formats used to process the sequence entries and trying to remember what their specific field codes mean. If you survive by surrounding yourself with well-thumbed hard copies...

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Customer Reviews

2 ratings

from a bioinformatics student and programmer

I picked this book up at BioCon 2003 and, to be honest, I wasn't sure at first how useful it was going to be. Flipping through a few of the sections, it seemed to be little more than an assemblage of man pages for each of the tools and programs it covered. So I put it on a shelf above my monitor at work for a while and as the days went by I found myself grabbing it more and more often to look something up. For example, I found myself needing reminding of the option for tabular output when doing a psi-blast. Grab the book ... a ha! ... -m 8. You can use the man pages or tutorials for many of things like this but sometimes there is a lot to wade through to find what you were looking for. Also, if you're like me you like the feel of a book sometimes and the ability to scrawl notes in the margins. It's just nice having all the options right there on the page.To be fair to the authors, I don't think that Chia-hsiu Tu was very accurate in his review by saying that "this books focus on EMBOSS only" (sic). EMBOSS coverage does make up about 58% of the book, but it is a suite of 150 useful programs. Unless you want only a sentence or two about each one you're going to have to use up a few pages. You get just enough info to learn about each and a quick guide to their usage. If you want to know more, there are links to their full documentation online.Some sections are stronger than others. The MEME/MAST chapter, for instance, doesn't just list out options but has great command line examples and a paragraph for each explaining what is going on. On the other hand, I wanted to use stretcher (in the EMBOSS package) and there was only a quick example (the syntax of which didn't work for me) and a listing of six options. I needed to find out how to make it work in a non-interactive way and write its output to STDOUT, neither of which were illustrated (-auto and -stdout, by the way).Ok, let's get to what this book covers. The first section goes really in depth to cover the data-exchange formats that we nerds find ourselves writing parsing scripts for all the time. (yes, yes, bioperl, biojava, etc. are great, but they aren't in this book. Hopefully one will cover them soon.) What I found most useful were the example files for each format (EMBL, DDBJ, Genbank, FASTA, SWISS-PROT, PFAM, & PROSITE) and the tables that were laid out for them. For example, there are nice little tables listing every feature (62 at my count) and feature qualifier (74!) that you can expect to find in a DDBJ/EMBL/Genbank file. And for each of those there is a little descripton of what they represent. Very nice.The second part of the book covers these specific tools: ReadSeq, the BLAST suite (7 progs), BLAT, CLUSTALW, HMMER (10 progs), MEME, MAST, and the EMBOSS suite (~150 progs). These sections are pretty decent and while you won't find much info on how the algorithms behind the programs work, you will have everything you need to run the programs and fine-tune their

an excellent rteference book

This books focus on EMBOSS only, a high quality open source bioinformatic toolkit. It can be a useful reference book when write web interface of those programs in this book. Also it provides the urls where we can download from? where the original idea come from?
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