Isbn: 9780896033580 - sequence data analysis guidebook (methods in molecular biology, 70, band 70) (6 Ergebnisse)

Zustand: Good. Good condition. Volume 70. A copy that has been read but remains intact. May contain markings such as bookplates, stamps, limited notes and highlighting, or a few light stains.

Zustand: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,800grams, ISBN:9780896033580. …

Zustand: New. In English.

Gebunden. Zustand: New. Computers 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 bec.

Zustand: New. Summaraizes methods for successfully using sequence analysis software packages. This work shows how to examine the data produced by automated sequencers, how to assess its quality, how to remove extraneous data, how to align multiple overlapping sequence fragments for either assembly into sequence contigs or comparison with similar sequences. Series: Methods in Molecular Biology. Num Pages: 324 pages, biography. BIC Classification: PDN; PSF; UY. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 229 x 148 x 20. Weight in Grams: 653. . 1996. Hardback. . . . . Books ship from the US and Ireland.…

Buch. Zustand: Neu. Neuware - Leading researchers concisely summarize their hands-on experiences and methods for successfully using the most popular sequence analysis software packages available. These experts demonstrate how to examine the data produced by modern automated sequencers, how to assess its quality, how to remove extraneous data, how to align multiple overlapping sequence fragments for either assembly into sequence contigs or comparison with similar sequences from different sources. Procedures for comparing newly derived sequences with the massive amounts of information in the sequence databases are fully covered, as are techniques for performing restriction analysis, searching for open reading frames, calculating the translation products of open reading frames, and making detailed analyses of the expressed 'proteins.'.…