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Copy Number Variants

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Cover of 'Copy Number Variants'

Table of Contents

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    Book Overview
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    Chapter 1 Identification of Copy Number Variants from SNP Arrays Using PennCNV
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    Chapter 2 Using SAAS-CNV to Detect and Characterize Somatic Copy Number Alterations in Cancer Genomes from Next Generation Sequencing and SNP Array Data
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    Chapter 3 Statistical Detection of Genome Differences Based on CNV Segments
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    Chapter 4 Whole-Genome Shotgun Sequence CNV Detection Using Read Depth
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    Chapter 5 Read Depth Analysis to Identify CNV in Bacteria Using CNOGpro
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    Chapter 6 Using HaMMLET for Bayesian Segmentation of WGS Read-Depth Data
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    Chapter 7 Split-Read Indel and Structural Variant Calling Using PINDEL
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    Chapter 8 Detecting Small Inversions Using SRinversion
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    Chapter 9 Detection of CNVs in NGS Data Using VS-CNV
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    Chapter 10 Structural Variant Breakpoint Detection with novoBreak
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    Chapter 11 Use of RAPTR-SV to Identify SVs from Read Pairing and Split Read Signatures
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    Chapter 12 Versatile Identification of Copy Number Variants with Canvas
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    Chapter 13 A Randomized Iterative Approach for SV Discovery with SVelter
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    Chapter 14 Analysis of Population-Genetic Properties of Copy Number Variations
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    Chapter 15 Validation of Genomic Structural Variants Through Long Sequencing Technologies
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    Chapter 16 Structural Variation Detection and Analysis Using Bionano Optical Mapping
Attention for Chapter 8: Detecting Small Inversions Using SRinversion
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Chapter title
Detecting Small Inversions Using SRinversion
Chapter number 8
Book title
Copy Number Variants
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8666-8_8
Pubmed ID
Book ISBNs
978-1-4939-8665-1, 978-1-4939-8666-8
Authors

Ruoyan Chen, Yu Lung Lau, Wanling Yang, Chen, Ruoyan, Lau, Yu Lung, Yang, Wanling

Abstract

Rapid development of next generation sequencing (NGS) technology has substantially improved our ability to detect genomic variations. However, unlike other variations, such as point mutations, insertions, and deletions, which can be identified in high sensitivities and specificities based on NGS reads, most of inversions, especially those shorter than 1 kb, remain difficult to detect. Here we introduce a new framework, SRinversion, which was developed specifically for detection of inversions shorter than 1 kb by splitting and realigning poorly mapped or unmapped reads of the NGS data.