VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics

Journal article

Open access

Peer reviewed

Yana Bromberg, Emidio Capriotti and Hannah Carter

BMC genomics, Vol.17 Suppl 2(Suppl 2), pp.425-425

06/23/2016

PMCID: PMC4928159

PMID: 27357578

Abstract

Alzheimer Disease - genetics

Congresses as Topic

Evolution, Molecular

Genomic Structural Variation

Humans

Ireland

Neoplasms - genetics

Phenotype

Polymorphism, Single Nucleotide

Precision Medicine

Protein Kinases - genetics

Protein Stability

Regulatory Sequences, Nucleic Acid

url

https://doi.org/10.1186/s12864-016-2721-3View

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Title: VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics
Creators: Yana Bromberg - Department of Genetics, Rutgers University, Lipman Hall 218, 08901, New Brunswick, NJ, USA. yanab@rci.rutgers.edu
Emidio Capriotti - Institute for Mathematical Modeling of Biological Systems, Department of Biology, Heinrich Heine University Düsseldorf, Universitaetsstr. 1, 40225, Düsseldorf, Germany. emidio.capriotti@hhu.de
Hannah Carter - Division of Medical Genetics, Department of Medicine, University of California, San Diego, 9500 Gilman Dr., 92093, La Jolla, CA, USA. hkcarter@ucsd.edu
Publication Details: BMC genomics, Vol.17 Suppl 2(Suppl 2), pp.425-425
Date published: 06/23/2016
Academic Unit: Biochemistry and Microbiology (SEBS)
Language: English
Resource Type: Journal article
Identifiers: 991031665615804646