Systematic Pharmacogenomics Analysis of a Malay Whole Genome: Proof of Concept for Personalized Medicine

Sequencing and analysis of a South Asian-Indian personal genome

(2012) Ravi Gupta et al.   BMC GENOMICS

Whole-Genome Sequencing in Personalized Therapeutics

(2012) P Cordero et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Systematic analysis and functional annotation of variations in the genome of an Indian individual

(2012) Ashok Patowary et al.   HUMAN MUTATION

CYP 2D6 polymorphism: A predictor of susceptibility and response to chemoradiotherapy in head and neck cancer

(2012) Pragya Shukla et al.   Journal of Cancer Research and Therapeutics

Interplay of pharmacogenetic variations in ABCB1 transporters and cytochrome P450 enzymes

(2011) Hee-Doo Yoo et al.   ARCHIVES OF PHARMACAL RESEARCH

The variant call format and VCFtools

(2011) P. Danecek et al.   BIOINFORMATICS

SNPedia: a wiki supporting personal genome annotation, interpretation and analysis

(2011) Michael Cariaso et al.   NUCLEIC ACIDS RESEARCH

Population Genetic Structure of Peninsular Malaysia Malay Sub-Ethnic Groups

(2011) Wan Isa Hatin et al.   PLoS One

PathwayAccess: CellDesigner plugins for pathway databases

(2010) J. L. Van Hemert et al.   BIOINFORMATICS

Population genetic inference from genomic sequence variation

(2010) J. E. Pool et al.   GENOME RESEARCH

Complete Khoisan and Bantu genomes from southern Africa

(2010) Stephan C. Schuster et al.   NATURE

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing

(2010) Akihiro Fujimoto et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

SOBA: sequence ontology bioinformatics analysis

(2010) B. Moore et al.   NUCLEIC ACIDS RESEARCH

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Development of Personalized Tumor Biomarkers Using Massively Parallel Sequencing

(2010) R. J. Leary et al.   Science Translational Medicine

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine

(2009) Kensaku Kawamoto et al.   BMC Medical Informatics and Decision Making

The first Korean genome sequence and analysis: Full genome sequencing for a socio-ethnic group

(2009) S.-M. Ahn et al.   GENOME RESEARCH

PharmGKB: Understanding the Effects of Individual Genetic Variants

(2008) Katrin Sangkuhl et al.   DRUG METABOLISM REVIEWS

Keeping Up With the Next Generation

(2008) John R. ten Bosch et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

The complete genome of an individual by massively parallel DNA sequencing

(2008) David A. Wheeler et al.   NATURE

The diploid genome sequence of an Asian individual

(2008) Jun Wang et al.   NATURE

The impact of next-generation sequencing technology on genetics

(2008) Elaine R. Mardis   TRENDS IN GENETICS