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DNA Sequencing Protocols
By
Alison J. M. Hill (editor) and
Colin A. Graham (editor)
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Bibliographic Detail
Publisher
Humana Pr Inc
Publication date
January 1, 2001
Pages
256
Binding
Hardcover
Edition
2 sub
Book category
Adult Non-Fiction
ISBN-13
9780896037168
ISBN-10
0896037169
Dimensions
0.75 by 6.25 by 9.50 in.
Weight
1.25 lbs.
Original list price
$104.50
Summaries and Reviews
(view table of contents)
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
The price comparison is for this edition
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.
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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