Copy Number Variants

Methods and Protocols

Buch | Softcover

206 Seiten

2019 | Softcover reprint of the original 1st ed. 2018
Humana Press Inc. (Verlag)
978-1-4939-9359-8 (ISBN)

Artikel merken

This volume offers detailed step-by-step instructions to allow beginners and experts alike to run appropriate copy number variants (CNV) detection software on a dataset of choice and discern between false positive noise and true positive CNV signals. Chapters guide readers through single nucleotide polymorphism (SNP) chips, optical mapping assembly techniques, and current open-source programs specializing in CNV detection. 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, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

Authoritative and cutting-edge, Copy Number Variants: Methods and Protocols aims to provide guidance to Bioinformaticians and Molecular Biologists who are interested in identifying copy number variants (CNV) with a wide variety of experimental media

Identification of Copy Number Variants from SNP Arrays using PennCNV.- Using SAAS-CNV to Detect and Characterize Somatic Copy Number Alterations in Cancer Genomes from Next Generation Sequencing and SNP Array Data.- Statistical Detection of Genome Differences Based on CNV Segment.- Whole Genome Shotgun Sequence CNV Detection using Read Depth.- Read Depth Analysis to Identify CNV in Bacteria using CNOGpro.- Using HaMMLET for Bayesian Segmentation of WGS read-depth Data.- Split-Read InDel and Structural Variant Calling Using PINDEL.- Detecting Small Inversions using SRinversion.- Detection of CNVs in NGS data using VS-CNV.- Structural Variant Breakpoint Detection with novoBreak.- Use of RAPTR-SV to Identify SVs from Read Pairing and Split Read Signatures.- Versatile Identification of Copy Number Variants with Canvas.- Analysis of Population-genetic Properties of Copy Number Variations.- Validation of Genomic Structural Variants through Long Sequencing Technologies.- Structural Variation Detection and Analysis using Bionano Optical Mapping.

Erscheinungsdatum	05.09.2019
Reihe/Serie	Methods in Molecular Biology ; 1833
Zusatzinfo	25 Illustrations, color; 11 Illustrations, black and white; X, 206 p. 36 illus., 25 illus. in color.
Verlagsort	Totowa, NJ
Sprache	englisch
Maße	178 x 254 mm
Themenwelt	Mathematik / Informatik ► Informatik ► Theorie / Studium
	Informatik ► Weitere Themen ► Bioinformatik
	Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie
Schlagworte	aCGH • DeAnnCNV • Melt • PBHoney • PINDEL
ISBN-10	1-4939-9359-3 / 1493993593
ISBN-13	978-1-4939-9359-8 / 9781493993598
Zustand	Neuware