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007			cr nn 008mamaa
008			100301s1997 xxu| o |||| 0|eng d
020			_a9781592595563
024	7		_a10.1385/0896033589 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC
050		4	_aQP624 _b1997 EB
245	0	0	_aSequence Data Analysis Guidebook _cedited by Simon R. Swindell
250			_a1st edition 1997
264		1	_aTotowa, NJ _bHumana Press _c1997
300			_a1 recurso en línea (IX, 324 páginas)
336			_atexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
347			_aarchivo de texto _bPDF
490	0		_aMethods in Molecular Biology _x1940-6029 _v70
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.
988			_aSpringer_Protocols_1997
650		7	_2embne _9140806 _aADN
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 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942			_2lcc _cLE
998			_b12/2023 _dz _eb _zSI