Variant Calling: Methods and Protocols

Author:   Charlotte Ng ,  Salvatore Piscuoglio
Publisher:   Springer-Verlag New York Inc.
Edition:   1st ed. 2022
Volume:   2493
ISBN:  

9781071622926


Pages:   354
Publication Date:   26 June 2022
Format:   Hardback
Availability:   Manufactured on demand   Availability explained
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Variant Calling: Methods and Protocols


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Author:   Charlotte Ng ,  Salvatore Piscuoglio
Publisher:   Springer-Verlag New York Inc.
Imprint:   Springer-Verlag New York Inc.
Edition:   1st ed. 2022
Volume:   2493
Weight:   0.889kg
ISBN:  

9781071622926


ISBN 10:   1071622927
Pages:   354
Publication Date:   26 June 2022
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

Data Processing and Germline Variant Calling with the Sentieon pipeline.- MuSE: A Novel Approach to Mutation Calling with Sample-Specific Error Modeling.- Octopus: Genotyping and Haplotyping in Diverse Experimental Designs.- Accurate Ensemble Prediction of Somatic Mutations with SMuRF2.- Detecting Medium and Large Insertions and Deletions with Transindel.- DECoN: A detection and visualisation tool for exonic copy number variants.- FACETS: Fraction and Allele-Specific Copy Number Estimates from Tumor Sequencing.- Meerkat: An Algorithm to Reliably Identify Structural Variations and Predict Their Forming Mechanisms.- Structural Variant Detection from Long-Read Sequencing Data with cuteSV.- Identifying Somatic Mitochondrial DNA Mutations.- Identification, Quantification, and Testing of Alternative Splicing Events from RNA-Seq data using SplAdder.- PipeIT: Somatic Variant Calling Workflow for Ion Torrent Sequencing Data.- Variant calling from RNA-seq data using the GATK joint genotyping workflow.- UMI-Varcal: a low-frequency variant caller for UMI-tagged paired-end sequencing data .- Alignment-free genotyping of known variations with MALVA.- Kmer2SNP: Reference-free heterozygous SNP calling using k-mer frequency distributions.- Somatic Single Nucleotide Variant Calling from Single Cell DNA sequencing data using SCAN-SNV.- Copy Number Variation Detection by Single-Cell DNA sequencing with SCOPE.- Variant Annotation and Functional Prediction: SnpEff.- Annotating Cancer-Related Variants At Protein-Protein Interface with Structure-PPi.- Preanalytical Variables and Sample Quality Control For Clinical Variant Analysis. 

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