VarioWatch: providing large-scale and comprehensive annotations on human genomic variants in the next generation sequencing era

AnnTools: a comprehensive and versatile annotation toolkit for genomic variants

(2012) Vladimir Makarov et al.   BIOINFORMATICS

miRdSNP: a database of disease-associated SNPs and microRNA target sites on 3'UTRs of human genes

(2012) Andrew E Bruno et al.   BMC GENOMICS

SVA: software for annotating and visualizing sequenced human genomes

(2011) Dongliang Ge et al.   BIOINFORMATICS

A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)

(2011) Joanna Amberger et al.   HUMAN MUTATION

A framework for variation discovery and genotyping using next-generation DNA sequencing data

(2011) Mark A DePristo et al.   NATURE GENETICS

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

(2011) Michael Cariaso et al.   NUCLEIC ACIDS RESEARCH

Reorganizing the protein space at the Universal Protein Resource (UniProt)

(2011)   NUCLEIC ACIDS RESEARCH

GenBank

(2011) D. A. Benson et al.   NUCLEIC ACIDS RESEARCH

CandiSNPer: a web tool for the identification of candidate SNPs for causal variants

(2010) A. O. Schmitt et al.   BIOINFORMATICS

pfSNP: An integrated potentially functional SNP resource that facilitates hypotheses generation through knowledge syntheses

(2010) Jingbo Wang et al.   HUMAN MUTATION

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

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

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

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

(2009) L. A. Hindorff et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms

(2008) C. Chelala et al.   BIOINFORMATICS

Functional analysis of novel SNPs and mutations in human and mouse genomes

(2008) Chuan-Kun Liu et al.   BMC BIOINFORMATICS

GenoWatch: a disease gene mining browser for association study

(2008) Y.-H. Chen et al.   NUCLEIC ACIDS RESEARCH

The GOA database in 2009--an integrated Gene Ontology Annotation resource

(2008) D. Barrell et al.   NUCLEIC ACIDS RESEARCH

NCBI Reference Sequences: current status, policy and new initiatives

(2008) K. D. Pruitt et al.   NUCLEIC ACIDS RESEARCH