Deep Sequencing Data Analysis / edited by Noam Shomron
Material type:
E-bookSeries: (Methods in Molecular Biology, 1940-6029; 2243).Publisher: New York, NY : Springer International Publising, 2021Edition: 2nd edition 2021.Description: 1 recurso en línea (X, 374 páginas) : 92 ilustraciones, 81 ilustraciones a color.ISBN: 9781071611036.Subject: Nucleótidos -- Manuales de laboratorio
| Item type | Current library | Collection | Call number | Status | Date due | Barcode | Item holds | |
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LIBRO-E NO PRÉSTAMO
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Madrid Digital Acceso Electrónico (UEM) | Ciencias e Ingeniería | QP625 .N89 2021 EB (Browse shelf(Opens below)) | Acceso electrónico | eBook.20122559 |
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| QP625 .N89 2019 EB Single Molecule and Single Cell Sequencing | QP625 .N89 2020 EB Microbial Cyclic Di-Nucleotide Signaling | QP625 .N89 2020 EB Trinucleotide Repeats : Methods and Protocols | QP625 .N89 2021 EB Deep Sequencing Data Analysis | QP625 .N89 2022 EB DNA and RNA Isolation Techniques for Non-Experts | QP625.N89 A383 2015 EB Advances in the Understanding of Biological Sciences Using Next Generation Sequencing (NGS) Approaches | QP625.N89 F545 2016 EB Field Guidelines for Genetic Experimental Designs in High-Throughput Sequencing |
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 Analysis to 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. .
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.
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