Computational Exome and Genome Analysis
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A01=Marten Jager
A01=Peter N. Robinson
A01=Rosario Michael Piro
Age Group_Uncategorized
Age Group_Uncategorized
Annotate VCF File
Array CGH
Author_Marten Jager
Author_Peter N. Robinson
Author_Rosario Michael Piro
automatic-update
Autosomal Recessive Disease
BAM File
Base Quality Score
Bed File
bioinformatics pipeline
bionformatics
Category1=Non-Fiction
Category=PS
Category=PSAK
Category=PSAK1
Category=PSAX
clinical genomics methods
computational variant prioritisation
COP=United States
Damian Smedley
Delivery_Delivery within 10-20 working days
Dominik Seelow
eq_bestseller
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_science
Exome Sequencing
FASTQ Files
FASTQ Format
Forward Strand
genetic variant analysis
Heterozygous Variant
Info Field
Jochen Hecht
Johannes Zschocke
Julius O.B. Jacobsen
Language_English
Manuel Holtgrewe
Marten Jager
Max Schubach
Mendelian Disease
NA12878 Exome
next generation sequencing
NGS
PA=Available
Paired End Reads
Paired End Sequences
PCR Duplicate
Peter Hansen
Peter Krawitz
Peter Robinson
Price_€100 and above
Prioritizing Candidate Genes
Protein Protein Interaction Network
PS=Active
rare disease genomics
Reference Genome
Rosario M. Piro
Sebastian Kohler
sequence data interpretation
SNV.
softlaunch
Tomasz Zemo jtel
VAF
Variant Call
VCF
VCF File
WES
WGS
Product details
- ISBN 9781498775984
- Weight: 1111g
- Dimensions: 156 x 234mm
- Publication Date: 11 Sep 2017
- Publisher: Taylor & Francis Inc
- Publication City/Country: US
- Product Form: Hardback
- Language: English
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Exome and genome sequencing are revolutionizing medical research and diagnostics, but the computational analysis of the data has become an extremely heterogeneous and often challenging area of bioinformatics. Computational Exome and Genome Analysis provides a practical introduction to all of the major areas in the field, enabling readers to develop a comprehensive understanding of the sequencing process and the entire computational analysis pipeline.
Peter Robinson is Professor for Medical Genomics at the Charité Universitätsmedizin Berlin, and professor for Bioinformatics at the Free University of Berlin. He studied Mathematics and Computer Science at Columbia University as well as Medicine at the University of Pennsylvania. Peter has led a bioinformatics research group since 2004. He has led the development of the Human Phenotype Ontology, which is used internationally to describe the clinical manifestations of patients with genetic disorders and to empower exome and genome analysis. His group has published algorithms for exome, genome, ChIP-seq and NGS T Cell Receptor profiling.
Rosario M. Piro is an Assistant Professor of Bioinformatics at Freie Universität Berlin and Charité-Universitätsmedizin Berlin, Germany. His research is mainly focused on computational neuropathology, including cancer genetics/genomics of brain tumors as well as network analysis and disease gene prediction for neurological disorders; and computational oncology in general, including the development and evolution of cancers in other organs or tissues. His expertise in next-generation sequencing data analysis techniques is complemented by a past research experience in the field of data-intensive distributed computing.
Marten Jäger is a graduate student in Peter Robinson’s group and has developed pipelines for exome and genome sequencing data. Marten’s work has involved the development of algorithms for variant annotation, exome prioritization, RNA-seq, and integrative genomics analysis.
