| 000 | 03512nam a22003735i 4500 | ||
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| 001 | 234563 | ||
| 003 | ES-VaUE | ||
| 005 | 20221220020610.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 100301s2001 xxu| s |||| 0|eng d | ||
| 020 | _a9781592591138 | ||
| 024 | 7 |
_a10.1385/1592591132 _2doi |
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| 040 |
_aES-MaUEC _bspa _cES-MaUEC |
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| 245 | 1 | 0 |
_aDNA Sequencing Protocols _cedited by Colin A Graham, Alison J.M. Hill. |
| 250 | _a2nd edition 2001 | ||
| 264 | 1 |
_aTotowa, NJ _bHumana Press _c2001 |
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| 300 |
_a1 recurso en línea (X, 244 páginas) _b33 ilustraciones |
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| 336 |
_atexto _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 347 |
_aarchivo de texto _bPDF |
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| 490 | 0 |
_aMethods in Molecular Biology _x1940-6029 _v167 |
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| 505 | 0 | _ato DNA Sequencing -- The Universal Primers and the Shotgun DNA Sequencing Method -- M13 Sequencing -- Primer Design and Primer-Directed Sequencing -- Direct Sequencing of DNA Produced in a Polymerase Chain Reaction -- Solid Phase Fluorescent Sequencing of the CFTR Gene -- Shotgun DNA Sequencing -- Cycle Sequencing -- Cycle Sequencing of Polymerase Chain Reaction-Amplified Genomic DNA with Dye-Labeled Universal Primers -- Automated Fluorescent DNA Sequencing on the ABI PRISM 377 -- Automated Fluorescent DNA Sequencing on the ABI PRISM 310 Genetic Analyzer -- Fluorescent Sequencing Protocols for the ALF -- Fluorescent Sequencing for Heterozygote Mutation Detection -- Sequence Databases and the Internet -- DNA Sequencing by Capillary Array Electrophoresis. | |
| 520 | _aSince the publication of the first edition of DNA Sequencing Protocols in 1993, major advances in its technology have made PCR-based semiautomated fluorescent sequencing the norm and enabled the complete sequencing of complex genomes. In DNA Sequencing Protocols, 2nd Edn., Colin Graham and a team of leading investigators and expert clinical scientists update the 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. Each method provides detailed, step-by-step instructions to ensure successful results, and includes helpful notes identifying and addressing potential problems. 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 impact today's genome sequencing projects, improve the accuracy and quality of DNA sequences obtained by smaller laboratories, and help lay the foundation for molecular diagnostics. | ||
| 700 | 1 |
_aGraham, Colin A _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 700 | 1 |
_aHill, Alison J.M _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 776 | 0 | 8 |
_iPrinted edition: _z9781489942128 |
| 776 | 0 | 8 |
_iPrinted edition: _z9781489942111 |
| 776 | 0 | 8 |
_iPrinted edition: _z9780896037168 |
| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/1592591132 _z(usuarios Universidad Europea de Valencia) |
| 942 |
_2lcc _cLE |
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| 988 | _aSpringer_Protocols_2001 | ||
| 999 |
_c234563 _d234563 |
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