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| 003 | ES-VaUE | ||
| 005 | 20221220020722.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 100301s1997 xxu| s |||| 0|eng d | ||
| 020 | _a9781592595563 | ||
| 024 | 7 |
_a10.1385/0896033589 _2doi |
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| 040 |
_aES-MaUEC _bspa _cES-MaUEC |
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| 245 | 1 | 0 |
_aSequence Data Analysis Guidebook _cedited by Simon R. Swindell. |
| 250 | _a1st edition 1997 | ||
| 264 | 1 |
_aTotowa, NJ _bHumana Press _c1997 |
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| 300 |
_a1 recurso en línea (IX, 324 páginas) _b |
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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 _v70 |
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| 505 | 0 | _aGeneJockeyll -- The Genetic Data Environment -- ABI Analysis -- SeqEd -- From ABI Sequence Data to LASERGENE's EDITSEQ -- SEQMAN -- GeneJockeyll -- AutoAssembler Sequence Assembly Software -- MEGALIGN -- GeneJockeyII -- GeneJockeyII -- Sequence Navigator -- The European Bioinformatics Institute -- GeneAssist -- GENEMAN of LASERGENE -- GeneJockeyII -- GeneJockeyII -- GeneJockeyII -- PROTEAN -- MAPDRAW -- The Gene Construction Kit -- GeneJockeyII -- OLIGO -- PRIME -- PRIMERSELECT -- The European Bioinformatics Institute. | |
| 520 | _aComputers have revolutionized the analysis of sequencing data. It is unlikely that any sequencing projects have been performed in the last few years without the aid of computers. Recently their role has taken a further major step forward. Computers have become smaller and more powerful and the software has become simpler to use as it has grown in sophistication. This book reflects that change since the majority of packages described here are designed to be used on desktop computers. Computer software is now available that can run gels, collect data, and assess its accuracy. It can assemble, align, or compare multiple fragments, perform restriction analyses, identify coding regions and specific motifs, and even design the primers needed to extend the sequencing. Much of this soft ware may now be used on relatively inexpensive computers. It is now possible to progress from isolate d DNA to database submission without writing a single base down. To reflect this progression, the chapters in our Sequence Data Analysis Guidebook are arranged, not by software package, but by fimction. The early chapters deal with examining the data produced by modem automated sequenc ers, assessing its quality, and removing extraneous data. The following chap ters describe the process of aligning multiple sequences in order to assemble overlapping fragments into sequence contigs to compare similar sequences from different sources. Subsequent chapters describe procedures for compar ing the newly derived sequence to the massive amounts of information in the sequence databases. | ||
| 700 | 1 |
_aSwindell, Simon R _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt |
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| 776 | 0 | 8 |
_iPrinted edition: _z9781489943385 |
| 776 | 0 | 8 |
_iPrinted edition: _z9780896033580 |
| 776 | 0 | 8 |
_iPrinted edition: _z9781489943378 |
| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/0896033589 _z(usuarios Universidad Europea de Valencia) |
| 942 |
_2lcc _cLE |
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| 988 | _aSpringer_Protocols_1997 | ||
| 999 |
_c235725 _d235725 |
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