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By
Colin A. Graham (editor) and
Alison J. M. Hill (editor)
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Bibliographic Detail
Publisher
Humana Pr Inc
Publication date
December 12, 2011
Pages
244
Binding
Paperback
Edition
2
Book category
Adult Non-Fiction
ISBN-13
9781617371509
ISBN-10
1617371505
Dimensions
0.50 by 6 by 9 in.
Weight
0.80 lbs.
Published in
Europe
Original list price
$149.00
Other format details
sci/tech
Summaries and Reviews
Amazon.com description: Product Description: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease. This second edition offers new material on automated DNA sequencers, capillary DNA sequencers, heterozygote mutation detection, web-based sequencing databases and genome sequencing sites, and the human genome project. State-of-the-art and highly practical, DNA Sequencing Protocols, 2nd Edn. constitutes an essential laboratory handbook for geneticists and molecular biologists, offering concise, easy-to-follow methods that will work and impact today's genome sequencing projects.
Editions
Hardcover
2 sub edition from Humana Pr Inc (January 1, 2001)
9780896037168 | details & prices | 256 pages | 6.25 × 9.50 × 0.75 in. | 1.25 lbs | List price $104.50
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
Paperback
2 edition from Humana Pr Inc (September 1, 2013)
9781489942128 | details & prices | 244 pages | 6.00 × 9.00 × 0.75 in. | 0.85 lbs | List price $99.00
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
The price comparison is for this edition
2 edition from Humana Pr Inc (December 12, 2011)
9781617371509 | details & prices | 244 pages | 6.00 × 9.00 × 0.50 in. | 0.80 lbs | List price $149.00
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
2 spi edition from Humana Pr Inc (January 1, 2001)
9780896037212 | details & prices | 6.50 × 9.00 × 0.75 in. | 0.95 lbs | List price $149.00
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
About: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
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