Results 41 to 50 of about 5,928,974 (349)

Public participation in genetic databases: crossing the boundaries between biobanks and forensic DNA databases through the principle of solidarity

open access: yesJournal of Medical Ethics, 2015
The ethical aspects of biobanks and forensic DNA databases are often treated as separate issues. As a reflection of this, public participation, or the involvement of citizens in genetic databases, has been approached differently in the fields of ...
H. Machado, Susana Silva
semanticscholar   +1 more source

326 Integrated Analysis of Genetic Databases Identifies miRNA Associated With Poor Survival In Melanoma

open access: yesJournal of Clinical and Translational Science, 2022
OBJECTIVES/GOALS: Despite advances in precision medicine and understanding of the molecular pathways, melanoma remains the deadliest skin cancer, warranting identification of novel biomarkers.
Reid McCallister   +3 more
doaj   +1 more source

Guilt By Genetic Association: The Fourth Amendment and the Search of Private Genetic Databases by Law Enforcement [PDF]

open access: yes, 2019
Over the course of 2018, a number of suspects in unsolved crimes have been identified through the use of GEDMatch, a public online genetic database. Law enforcement’s use of GEDMatch to identify suspects in cold cases likely does not constitute a search ...
Abrahamson, Claire
core   +1 more source

Variants within the MMP3 gene are associated with achilles tendinopathy: possible interaction with the COL5A1 gene [PDF]

open access: yes, 2009
Objectives: Sequence variation within the COL5A1 and TNC genes are known to associate with Achilles tendinopathy. The primary aim of this case-control genetic association study was to investigate whether variants within the matrix metalloproteinase 3 ...
Collins, M   +5 more
core   +1 more source

Human Ageing Genomic Resources: new and updated databases

open access: yesNucleic Acids Res., 2017
In spite of a growing body of research and data, human ageing remains a poorly understood process. Over 10 years ago we developed the Human Ageing Genomic Resources (HAGR), a collection of databases and tools for studying the biology and genetics of ...
Robi Tacutu   +11 more
semanticscholar   +1 more source

Estimation of ENPP1 deficiency genetic prevalence using a comprehensive literature review and population databases

open access: yesOrphanet Journal of Rare Diseases, 2022
Background ENPP1 Deficiency—caused by biallelic variants in ENPP1—leads to widespread arterial calcification in early life (Generalized Arterial Calcification of Infancy, GACI) or hypophosphatemic rickets in later life (Autosomal Recessive ...
Lauren M. Chunn   +6 more
doaj   +1 more source

Towards a bioinformatics platform for the Musa research community : [Abstract W076] [PDF]

open access: yes, 2010
Current experiments in genomics produce a large amount of data that needs to be organized into databases and broadly accessible. Like other species, the Musa genomics community would benefit from centralized and innovative ways to study its genome.
Argout, Xavier   +8 more
core  

Privacy in the Genomic Era [PDF]

open access: yes, 2015
Genome sequencing technology has advanced at a rapid pace and it is now possible to generate highly-detailed genotypes inexpensively. The collection and analysis of such data has the potential to support various applications, including personalized ...
Ayday, Erman   +7 more
core   +4 more sources

GSD: a genetic screen database

open access: yesMechanisms of Development, 2004
The systematic assignment of gene function to a sequenced genome is one of the outstanding challenges in the post-genomic era. Large-scale systematic mutagenesis screens are important tools for reaching this goal. Here we describe GSD, a software package that allows storage and integration of data from genetic screens. GSD was initially developed for a
Henrich, Thorsten   +6 more
openaire   +2 more sources

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

open access: yesNucleic Acids Res., 2004
Online Mendelian Inheritance in Man (OMIM™) is a comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
A. Hamosh   +4 more
semanticscholar   +1 more source

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