(Ilmumisaeg: 24-Mar-2023, Hardback, Kirjastus: Springer-Verlag New York Inc., ISBN-13: 9781071629734)
This detailed volume provides state-of-the-art methodologies and reviews of important topics in the field of homology modeling. From homology modeling in the twilight zone and improving accuracy through sequence space analysis to approaches to constr...Loe edasi...
(Ilmumisaeg: 04-Jan-2023, Hardback, Kirjastus: World Scientific Publishing Co Pte Ltd, ISBN-13: 9789811258572)
Machine Learning In Bioinformatics Of Protein Sequences Guides Readers Around The Rapidly Advancing World Of Cutting-Edge Machine Learning Applications In The Protein Bioinformatics Field. Edited By Bioinformatics Expert, Dr Lukasz Kurgan, And Wit...Loe edasi...
Genome sequencing has become a basic tool of plant and animal breeding. Reduced costs have allowed the sequencing of thousands of plant lines or cultivars, leading to previously unobtainable insights into genetic impacts during breeding and generatin...Loe edasi...
(Ilmumisaeg: 19-Feb-2022, Paperback / softback, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. K, ISBN-13: 9783662644720)
This book is a practical guide for biologists who use multiple sequence alignments (MSAs) for their data analysis and are looking for a comprehensive overview of the many different programs. Despite their important role in data analysis, there i...Loe edasi...
Population Genomics With R presents a multidisciplinary approach to the analysis of population genomics. The methods treated cover a large number of topics from traditional population genetics to large-scale genomics with high-thr...Loe edasi...
(Ilmumisaeg: 29-Jan-2018, Hardback, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319649177)
The authors present in this book a new general approach called parameter advising for finding a parameter setting that produces a high-quality alignment for a given set of input sequences. In this framework, a parameter advisor is a procedu...Loe edasi...
(Ilmumisaeg: 26-Aug-2016, Hardback, Kirjastus: John Wiley & Sons Inc, ISBN-13: 9781118229040)
This book uniquely provides a comprehensive view into recently developed large-scale alignment models and techniques while covering the current and future challenges of aligning multiple sequences. It provides detailed descriptions of the traditional...Loe edasi...
(Ilmumisaeg: 09-Jun-2016, Hardback, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319313481)
High throughput sequencing (HTS) technologies have conquered the genomics and epigenomics worlds. The applications of HTS methods are wide, and can be used to sequence everything from whole or partial genomes, Transcriptomes, non-coding RNAs, ribosom...Loe edasi...
This work covers sequence-based protein homology detection, a fundamental and challenging bioinformatics problem with a variety of real-world applications. The text first surveys a few popular homology detection methods, such as Position-Specific Sco...Loe edasi...
Geneticists and other biomedical researchers summarize next-generation sequencing (NGS) technologies and their application in selected fields of biomedical research. The topics include single nucleotide polymorphisms (SNP) assessment of draft genomes...Loe edasi...
(Ilmumisaeg: 30-Oct-2013, Hardback, Kirjastus: Humana Press Inc., ISBN-13: 9781627036450)
From basic performing of sequence alignment through a proficiency at understanding how most industry-standard alignment algorithms achieve their results, Multiple Sequence Alignment Methods describes numerous algorithms and their nuances in chapters...Loe edasi...
(Ilmumisaeg: 22-Aug-2011, Paperback / softback, Kirjastus: University of California Press, ISBN-13: 9780520271319)
saadame teile pakkumise kasutatud raamatule, mille hind võib erineda kodulehel olevast hinnast
The sequencing of the human genome involved thousands of scientists but used relatively few tools. Today, obtaining sequences is simpler, but aligning the sequences--making sure that sequences from one source are properly compared to those from other...Loe edasi...
(Ilmumisaeg: 11-Mar-2009, Hardback, Kirjastus: University of California Press, ISBN-13: 9780520256972)
saadame teile pakkumise kasutatud raamatule, mille hind võib erineda kodulehel olevast hinnast
The sequencing of the human genome involved thousands of scientists but used relatively few tools. Today, obtaining sequences is simpler, but aligning the sequences--making sure that sequences from one source are properly compared to those from other...Loe edasi...
Now spurred by advances in biochips and genome research, this relatively new field has grown dramatically from the days when it was primarily used to yield detailed, accurate information on the progress of disease in the population and service levels...Loe edasi...
