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Deep Sequencing Data Analysis -

Deep Sequencing Data Analysis

Noam Shomron (Herausgeber)

Buch | Softcover
374 Seiten
2022 | 2nd ed. 2021
Springer-Verlag New York Inc.
978-1-0716-1105-0 (ISBN)
CHF 194,70 inkl. MwSt
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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.
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. Chapters guide readers through techniques for processing RNA-seq data, microbiome analysis, deep learning methodologies, and various approaches for the identification of sequence variants. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.



 Authoritative and cutting-edge, Deep Sequencing Data Analysis: Methods and Protocols, Second Edition aims to ensure successful results in the further study of this vital field.

Detecting Causal Variants in Mendelian Disorders using Whole Genome Sequencing.- Statistical Considerations on NGS Data for Inferring Copy Number Variations.- Applications of Community Detection Algorithms to Large Biological Datasets.- Processing and Analysis of RNA-seq data from Public Resources.- Improved Analysis of High-throughput Sequencing Data Using Small Universal k-mer Hitting Sets.- An Introduction to Whole-metagenome Shotgun Sequencing Studies.- Microbiome Analysis using 16S Amplicon Sequencing: From Samples to ASVs.- RNA-Seq in Non-model Organisms.- Deep Learning Applied on Next Generation Sequencing Data Analysis.- Interrogating the Accessible Chromatin Landscape of Eukaryote Genomes using ATAC-seq.- Genome-Wide Noninvasive Prenatal Diagnosis of SNPs and Indels.- Genome-wide Noninvasive Prenatal Diagnosis of De Novo Mutations.- Accurate Imputation of Untyped Variants from Deep Sequencing Data.- Multi-region Sequence Analysisto Predict Intratumor Heterogeneity and Clonal Evolution.- Overcoming Interpretability in Deep Learning Cancer Classification.- Single-cell Transcriptome Profiling.- Biological Perspectives of RNA-sequencing Experimental Design.- Analysis of microRNA Regulation in Single Cells.- DNA Data Collection and Analysis in the Forensic Arena.



 




 

Erscheinungsdatum
Reihe/Serie Methods in Molecular Biology ; 2243
Zusatzinfo 81 Illustrations, color; 11 Illustrations, black and white; X, 374 p. 92 illus., 81 illus. in color.
Verlagsort New York, NY
Sprache englisch
Maße 178 x 254 mm
Themenwelt Mathematik / Informatik Informatik Theorie / Studium
Informatik Weitere Themen Bioinformatik
Naturwissenschaften Biologie Genetik / Molekularbiologie
Schlagworte Bioinformatics • ChIP-Seq • Forensics • Ion Torrent • Nanopore
ISBN-10 1-0716-1105-4 / 1071611054
ISBN-13 978-1-0716-1105-0 / 9781071611050
Zustand Neuware
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