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Titlebook: Bioinformatics and the Cell; Modern Computational Xuhua Xia Book 2018Latest edition Springer Science+Business Media LLC 2018 Proteomics.DNA

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發(fā)表于 2025-3-21 19:27:23 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Bioinformatics and the Cell
期刊簡稱Modern Computational
影響因子2023Xuhua Xia
視頻videohttp://file.papertrans.cn/188/187203/187203.mp4
發(fā)行地址First book with comprehensive numerical illustration of mathematical techniques and computational algorithms used in bioinformatics to convert the rapidly increasing molecular data into organized biol
圖書封面Titlebook: Bioinformatics and the Cell; Modern Computational Xuhua Xia Book 2018Latest edition Springer Science+Business Media LLC 2018 Proteomics.DNA
影響因子.This second edition integrates the more technical and mathematical aspects of bioinformatics with concrete examples of their application to current research problems in molecular, cellular and evolutionary biology. This broad, unified approach is made possible, in large part, by the very wide scope of Dr. Xia’s own research experience. The integration of genomics, proteomics and transcriptomics into a single volume makes this book required reading for anyone entering the new and emerging fields of Systems Biology and Evolutionary Bioinformatics..
Pindex Book 2018Latest edition
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書目名稱Bioinformatics and the Cell影響因子(影響力)




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,?u?ere Eigenschaften der Atomkerne,and match-mismatch matrices affect such parameters? What are the key algorithms for FASTA and BLAST? How do their differences affect sensitivity of sequence search? This chapter addresses these questions and illustrates applications of string matching in genomics, transcriptomics, and proteomics, as
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Streuprozesse und Kernreaktionen,stral-descendant relationships through molecular phylogenetics, and local alignment mainly for identifying sequence similarities that may be due to either inheritance or convergence. Dynamic programming algorithm for pairwise alignment and profile alignment is illustrated in detail, for both constan
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https://doi.org/10.1007/978-3-322-91795-9the sequences, but we do not know what the motif looks like or where it is located within each sequence. Gibbs sampler will find such a motif if it is well represented in these sequences. If we have a set of yeast intron sequences each containing a branchpoint site (BPS) somewhere, but we do not kno
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Der Atomkern als dynamisches System,rent transcription start and termination sites. It has also been used in ribosome profiling for characterizing translation efficiency and Hi-C method for constructing genome 3-D architecture. There are two main difficulties in analyzing HTS data: the large file size, often in terabytes, and the allo
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https://doi.org/10.1007/978-3-322-90950-3clustering co-expressed genes as a basis to infer co-regulated genes. It can be applied to any set of objects as long as a distance function can be defined between objects. SOM is numerically illustrated together with a simple UPGMA method to contrast between the two. A less known application of SOM
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