Biomedical data sharing is desirable, but problematic. Data "discovery" approaches-which establish the existence rather than the substance of data-precisely connect data owners with data seekers, and thereby promote data sharing. Cafe Variome (http://www.cafevariome.org) was therefore designed to provide a general-purpose, Web-based, data discovery tool that can be quickly installed by any genotype-phenotype data owner, or network of data owners, to make safe or sensitive content appropriately discoverable. Data fields or content of any type can be accommodated, from simple ID and label fields through to extensive genotype and phenotype details based on ontologies. The system provides a "shop window" in front of data, with main interfaces b...
Abstract Background With the advent of whole exome (ES) and genome sequencing (GS) as tools for dise...
<div><div><div><p>It is estimated 350 million people worldwide are afflicted with a rare disease. Be...
Background: Sharing of data about variation and the associated phenotypes is a critical need, yet va...
Biomedical data sharing is desirable, but problematic. Data "discovery" approaches-which establish t...
This paper describes an information technology, infrastructure aimed at supporting translational bio...
Background: Linking genotypic and phenotypic information is one of the greatest challenges of curren...
<p>The availability of low-cost genome sequencing has allowed for the identification of the molecula...
There are few better examples of the need for data sharing than in the rare disease community, where...
There are few better examples of the need for data sharing than in the rare disease community, where...
There are few better examples of the need for data sharing than in the rare disease community, where...
This paper describes the application of an information technology infrastructure aimed at supporting...
Summary: Large biobanks linking phenotype to genotype have led to an explosion of genetic associatio...
Advances in next-generation sequencing (NGS) technologies have helped reveal causal variants for gen...
International audienceABSTRACT: BACKGROUND: Sharing of data about variation and the associated pheno...
ABSTRACT Objectives To build a searchable database for SNP array data from the GoDARTS data set, ...
Abstract Background With the advent of whole exome (ES) and genome sequencing (GS) as tools for dise...
<div><div><div><p>It is estimated 350 million people worldwide are afflicted with a rare disease. Be...
Background: Sharing of data about variation and the associated phenotypes is a critical need, yet va...
Biomedical data sharing is desirable, but problematic. Data "discovery" approaches-which establish t...
This paper describes an information technology, infrastructure aimed at supporting translational bio...
Background: Linking genotypic and phenotypic information is one of the greatest challenges of curren...
<p>The availability of low-cost genome sequencing has allowed for the identification of the molecula...
There are few better examples of the need for data sharing than in the rare disease community, where...
There are few better examples of the need for data sharing than in the rare disease community, where...
There are few better examples of the need for data sharing than in the rare disease community, where...
This paper describes the application of an information technology infrastructure aimed at supporting...
Summary: Large biobanks linking phenotype to genotype have led to an explosion of genetic associatio...
Advances in next-generation sequencing (NGS) technologies have helped reveal causal variants for gen...
International audienceABSTRACT: BACKGROUND: Sharing of data about variation and the associated pheno...
ABSTRACT Objectives To build a searchable database for SNP array data from the GoDARTS data set, ...
Abstract Background With the advent of whole exome (ES) and genome sequencing (GS) as tools for dise...
<div><div><div><p>It is estimated 350 million people worldwide are afflicted with a rare disease. Be...
Background: Sharing of data about variation and the associated phenotypes is a critical need, yet va...