The book by Dale, Von Schantz and Platt, From Genes to Genomes, is almost perfect. It is a 350 or so page exceptionally well written
book describing all the introductory materials one would need to become current
with genomes and genomics efforts. As with many of the other books I had around
I first looked at this and at a glance set it aside. Then came the moment when
I wanted to re-understand something and I opened this book up and I was hooked.
It in a clean and clear manner takes the reader from basic DNA principles and
through all of the key techniques used in genomic studies today. It avoids
getting to complex into any one area and it reads in a straightforward and
consistent manner. It is a superb asset for “catching up” and I suspect for first
learning the materials.
Chapter 1 is the basic introduction to genes and genomes. It
is DNA 101 but it contains little tidbits of essential materials that are all
well integrated. One thus starts with a clear understanding where the authors
are taking the reader.
Chapter 2 is the material on basic gene cloning. It uses the
plasmid approach with bacteriophage and does so without burdening the reader
with too much overhead and history. This Chapter discusses technique and
technology and the reader is given a logical approach to the basics of cloning.
Restriction enzymes are introduced and the material is adequate to have enough
depth to see how they can be applied. There are, of course, a lot of
implementation questions that are left hanging but that is typical of this
study. There is a section on ligation and I would like to have seen this
carried over a bit when discussing gene knock-outs. We can understand how the
genes ligate but the question is how well does this carry-over the later
processes.
Chapter 3 discusses DNA libraries. This is a wonderful
summary of the concept. The graphics supplement the text without over powering
it. One example of what I call the cook book facts is demonstrated in p 95 when
discussing hybridization. Here is the curve showing how as temperature
increases the DNA starts to break apart. This is the denaturing of DNA, a
concept again used with the PCR analysis. This is less a theoretical or
structure issue but one of those cook-book facts that have been added to the
tool chest of the Genome builder.
Chapter 4 is the PCR process. Simply it is the separating of
DNA, then tagging one end and the other end and going through a temperature
sensitive denaturing and rebuilding until what is left is millions of copies of
a desired DNA segment. My only complaint here is that the graphic, good, albeit
it could be made a bit better with color.
Chapter 5 discusses sequencing and it gives a superb
discussion of the Sanger approach. Namely ddNTPs are used with segments and
then measured in a gel electrophoresis. I assume that the reader may have had
some understanding of the physical details but overall it is clear and exceptionally
useful.
The text continues developing other elements used in current
day genomics. Chapter 9 is an attempt to provide an overview of microarrays,
SNP, and even GWAS and phylogenetics. My problem here is that they are trying
to stretch it a bit too far. These are reasonable summaries but to do
microarrays justice it may take a bit more detail, and yes color, and the
phylogenetics is much too much just a high level summary.
Finally the Glossary is fantastic and worth every page.
The strengths and weakness of the book are simple. On the
strength side it covers all the key issues superbly. On the negative side, and
this may be perhaps me, I find that almost like Organic Chemistry, in Gene
manipulation there still are many cookbook rules that are scattered between the
facts and logical constructs. If somehow there could be a clarification of the
cook book rule and the well understood logical steps that would be a help.
Overall I would highly recommend this book for almost
anyone, from beginner to professional. My focus is clinical and theoretical
modelling and analysis, and I have avoided bench work as much as possible. But
by reading this book I can see again how much work has been done over the past
few decades.