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Deep Sequencing Data Analysis, Shomron Noam


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Цена: 18167.00р.
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Автор: Shomron Noam
Название:  Deep Sequencing Data Analysis
ISBN: 9781071611029
Издательство: Springer
Классификация:


ISBN-10: 107161102X
Обложка/Формат: Hardcover
Страницы: 374
Вес: 0.82 кг.
Дата издания: 23.03.2021
Язык: English
Размер: 25.91 x 19.56 x 2.29 cm
Ссылка на Издательство: Link
Поставляется из: Германии
Описание: This second edition provides new and updated chapters from expert researchers in the field detailing methods used to study the multi-facet deep sequencing data field.


Clinical Applications for Next Generation Sequencing

Автор: Urszula Demkow
Название: Clinical Applications for Next Generation Sequencing
ISBN: 0128017392 ISBN-13(EAN): 9780128017395
Издательство: Elsevier Science
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Цена: 12462.00 р.
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Описание:

Clinical Applications for Next Generation Sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments.

Rooted in both medical genetics and clinical medicine, the book fills the gap between state-of-the-art technology and evidence-based practice, providing an educational opportunity for users to advance patient care by transferring NGS to the needs of real-world patients.

The book builds an interface between genetic laboratory staff and clinical health workers to not only improve communication, but also strengthen cooperation. Users will find valuable tactics they can use to build a systematic framework for understanding the role of NGS testing in both common and rare diseases and conditions, from prenatal care, like chromosomal abnormalities, up to advanced age problems like dementia.

Deep sequencing data analysis

Название: Deep sequencing data analysis
ISBN: 1627035133 ISBN-13(EAN): 9781627035132
Издательство: Springer
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Цена: 22359.00 р.
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Описание: This book details key data analysis procedures for deep sequencing data interpretation. It includes lists of necessary materials and reagents; step-by-step, readily reproducible protocols, and key tips on troubleshooting and avoiding known pitfalls.

Deep Sequencing Data Analysis

Автор: Noam Shomron
Название: Deep Sequencing Data Analysis
ISBN: 149396027X ISBN-13(EAN): 9781493960279
Издательство: Springer
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Цена: 14673.00 р.
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Описание: This book details key data analysis procedures for deep sequencing data interpretation. It includes lists of necessary materials and reagents; step-by-step, readily reproducible protocols, and key tips on troubleshooting and avoiding known pitfalls.

Sequencing Technologies In Microbial Food Safety And Quality /

Автор: Devarajan Thangardurai
Название: Sequencing Technologies In Microbial Food Safety And Quality /
ISBN: 0367351188 ISBN-13(EAN): 9780367351182
Издательство: Taylor&Francis
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Цена: 35218.00 р.
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Описание: This book reviews several practices in that NGS contributes to foodborne pathogens functional characterization, management and control. This book focuses on potential uses of sequencing technologies in microbial food safety and quality, also highlighting present challenges in the food industry.

Next Generation Sequencing and Data Analysis

Автор: Kappelmann-Fenzl Melanie
Название: Next Generation Sequencing and Data Analysis
ISBN: 3030624897 ISBN-13(EAN): 9783030624897
Издательство: Springer
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Цена: 11878.00 р.
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Описание: This textbook provides step-by-step protocols and detailed explanations for RNA Sequencing, ChIP-Sequencing and Epigenetic Sequencing applications.

Next Generation Sequencing & Applications

Автор: Preethi Kartan
Название: Next Generation Sequencing & Applications
ISBN: 1773611100 ISBN-13(EAN): 9781773611105
Издательство: Mare Nostrum (Eurospan)
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Цена: 20691.00 р.
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Описание: Billions of spots of tiny genetic code comprise the human genome. It was DNA sequencing technology that had revolutionized genomic research by decoding the valuable genetic information by giving the picture of an exact order of occurrence of nucleotides in a DNA. The inception of first-generation sequencing method, also called Sanger sequencing took place in 1975. The first major breakthrough of first-generation sequencing comes, when the 13 year log Human Genome Project (HGP) was completed in 2003 at a cost $3 million. With ever increasing demands of researchers and clinicians, complex genomic research require a depth of information which is however beyond the capacity of traditional DNA sequencing technologies. These research questions gaps are very well addressed by Next-generation sequencing (NGS) has filled that gap of cheaper as well as faster sequencing technology.It is just a decade old technology, but it has popularize the next-generation sequencing to high-throughput sequencing hat allow millions to trillions of observations to be made in parallel during a single instrument run. Since the introduction of these technologies, the number of applications and methods that influence the power of genome-scale sequencing has increased exponentially. Although in genome research NGS has mostly superseded conventional Sanger sequencing, it has not yet translated into routine clinical practice.The following chapter will highlight the concepts, technologies, and methods of next-generation sequencing to illustrate the breadth and depth of the applications and research areas that are driving progress in genomics.

Single Molecule and Single Cell Sequencing

Автор: Suzuki
Название: Single Molecule and Single Cell Sequencing
ISBN: 9811360367 ISBN-13(EAN): 9789811360367
Издательство: Springer
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Цена: 22359.00 р.
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Описание: This book presents an overview of the recent technologies in single molecule and single cell sequencing. New developments and technologies are constantly emerging, which will further expand sequencing applications. In parallel, single cell sequencing technologies are rapidly becoming a popular platform.

Hidden Treasures in Contemporary RNA Sequencing

Автор: Serghei Mangul; Harry Taegyun Yang; Eleazar Eskin;
Название: Hidden Treasures in Contemporary RNA Sequencing
ISBN: 3030139727 ISBN-13(EAN): 9783030139728
Издательство: Springer
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Цена: 6986.00 р.
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Описание:

Advances in RNA-sequencing (RNA-seq) technologies have provided an unprecedented opportunity to explore the gene expression landscape across individuals, tissues, and environments by efficiently profiling the RNA sequences present in the samples. When a reference genome sequence or a transcriptome of the sample is available, mapping-based RNA-seq analysis protocols align the RNA-seq reads to the reference sequences, identify novel transcripts, and quantify the abundance of expressed transcripts.
The reads that fail to map to the human reference, known as unmapped reads, are a large and often overlooked output of standard RNA-seq analyses. Even in carefully executed experiments, the unmapped reads can comprise a considerable fraction of the complete set of reads produced, and can arise due to technical sequencing produced by low-quality and error-prone copies of the nascent RNA sequence being sampled. Reads can also remain unmapped due to unknown transcripts, recombined B and T cell receptor sequences, A-to-G mismatches from A-to-I RNA editing, trans-splicing, gene fusion, circular RNAs, and the presence of non-host RNA sequences (e.g. bacterial, fungal, and viral organisms). Unmapped reads represent a rich resource for the study of B and T cell receptor repertoires and the human microbiome system—without incurring the expense of additional targeted sequencing.
This book introduces and describes the Read Origin Protocol (ROP), a tool that identifies the origin of both mapped and unmapped reads. The protocol first identifies human reads using a standard high-throughput algorithm to map them onto a reference genome and transcriptome. After alignment, reads are grouped into genomic (e.g. CDS, UTRs, introns) and repetitive (e.g. SINEs, LINEs, LTRs) categories. The rest of the ROP protocol characterizes the remaining unmapped reads, which failed to map to the human reference sequences.
Next Generation Sequencing in Forensic Science: A Primer

Автор: Elkins Kelly M., Zeller Cynthia B.
Название: Next Generation Sequencing in Forensic Science: A Primer
ISBN: 1032072040 ISBN-13(EAN): 9781032072043
Издательство: Taylor&Francis
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Цена: 8726.00 р.
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Описание: Next Generation Sequencing in Forensic Science prepares practitioners and students to utilize and implement this new technology into their lab casework for forensic investigations, highlighting early applications of how NGS results have been used in court.

De-Sequencing: Identity Work with Genes

Автор: Mahr Dana, Von Arx Martina
Название: De-Sequencing: Identity Work with Genes
ISBN: 9811577277 ISBN-13(EAN): 9789811577277
Издательство: Springer
Цена: 13974.00 р.
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Описание: The book unpacks this type of `sequence-speech` in engaging detail, adopting a personal, social, cultural, and bio-political approach to examine the transformation of human identity and reflexivity in the era of genetic citizenship.

Algorithms for Next-Generation Sequencing Data

Автор: Mourad Elloumi
Название: Algorithms for Next-Generation Sequencing Data
ISBN: 3319867105 ISBN-13(EAN): 9783319867106
Издательство: Springer
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Цена: 13974.00 р.
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Описание: The 14 contributed chapters in this book survey the most recent developments in high-performance algorithms for NGS data, offering fundamental insights and technical information specifically on indexing, compression and storage; error correction; alignment; and assembly. The book will be of value to researchers, practitioners and students engaged with bioinformatics, computer science, mathematics, statistics and life sciences.

DNA Sequencing Protocols

Автор: Graham Colin A.
Название: DNA Sequencing Protocols
ISBN: 1617371505 ISBN-13(EAN): 9781617371509
Издательство: Springer
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Цена: 18167.00 р.
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Описание: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.


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