000 04389nam a22005055i 4500
001 978-1-59259-556-3
003 DE-He213
005 20260610083715.0
007 cr nn 008mamaa
008 100301s1997 xxu| s |||| 0|eng d
020 _a9781592595563
_9978-1-59259-556-3
024 7 _a10.1385/0896033589
_2doi
050 4 _aQH573-671
072 7 _aPSF
_2bicssc
072 7 _aSCI017000
_2bisacsh
072 7 _aPSF
_2thema
082 0 4 _a571.6
_223
245 1 0 _aSequence Data Analysis Guidebook
_h[electronic resource] /
_cedited by Simon R. Swindell.
250 _a1st ed. 1997.
264 1 _aTotowa, NJ :
_bHumana Press :
_bImprint: Humana,
_c1997.
300 _aIX, 324 p.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 1 _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.
532 8 _aAccessibility summary: This PDF is not accessible. It is based on scanned pages and does not support features such as screen reader compatibility or described non-text content (images, graphs etc). However, it likely supports searchable and selectable text based on OCR (Optical Character Recognition). Users with accessibility needs may not be able to use this content effectively. Please contact us at accessibilitysupport@springernature.com if you require assistance or an alternative format.
532 8 _aInaccessible, or known limited accessibility
532 8 _aNo reading system accessibility options actively disabled
532 8 _aPublisher contact for further accessibility information: accessibilitysupport@springernature.com
650 0 _aCytology.
650 1 4 _aCell Biology.
700 1 _aSwindell, Simon R.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
710 2 _aSpringerLink (Online service)
773 0 _tSpringer Nature eBook
776 0 8 _iPrinted edition:
_z9780896033580
776 0 8 _iPrinted edition:
_z9781489943378
776 0 8 _iPrinted edition:
_z9781489943385
830 0 _aMethods in Molecular Biology,
_x1940-6029 ;
_v70
856 4 0 _uhttps://doi.org/10.1385/0896033589
912 _aZDB-2-PRO
999 _c8141
_d8141