Lista de obras - Juha Muilu - Dominio Público Uruguay

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

artículo científico publicado en 2012

A systems approach delivers a functional microRNA catalog and expanded targets for seizure suppression in temporal lobe epilepsy

scientific article published on 24 June 2020

ASD: the Alternative Splicing Database.

artículo científico publicado en 2004

Conservation of human alternative splice events in mouse

artículo científico publicado en 2003

Data Modeling and Data Communication in GenomEUtwin

Data modeling and data communication in GenomEUtwin.

artículo científico publicado en 2003

Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

artículo científico publicado en 2016

GBuilder--an application for the visualization and integration of EST cluster data.

artículo científico publicado en 2001

Genetics in an isolated population like Finland: a different basis for genomic medicine?

artículo científico publicado en 2017

Genotype-phenotype databases: challenges and solutions for the post-genomic era.

artículo científico publicado en 2009

Geographical structure and differential natural selection among North European populations

scientific article published on 05 March 2009

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

artículo científico publicado en 2017

Identity in research infrastructure and scientific communication: Report from the 1st IRISC workshop, Helsinki Sep 12-13, 2011

NordicDB: a Nordic pool and portal for genome-wide control data

artículo científico publicado en 2010

Observ-OM and Observ-TAB: Universal syntax solutions for the integration, search, and exchange of phenotype and genotype information

artículo científico publicado en 2012

Paradigm shifts in the approaches for gene annotation

article

The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.

artículo científico publicado en 2013

The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button

artículo científico publicado en 2010

The federated database--a basis for biobank-based post-genome studies, integrating phenome and genome data from 600,000 twin pairs in Europe

artículo científico publicado en 2007

The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation

artículo científico publicado en 2009

VarioML framework for comprehensive variation data representation and exchange

artículo científico publicado en 2012

Lista de obras de Juha Muilu

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

A systems approach delivers a functional microRNA catalog and expanded targets for seizure suppression in temporal lobe epilepsy

ASD: the Alternative Splicing Database.

Conservation of human alternative splice events in mouse

Data Modeling and Data Communication in GenomEUtwin

Data modeling and data communication in GenomEUtwin.

Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

GBuilder--an application for the visualization and integration of EST cluster data.

Genetics in an isolated population like Finland: a different basis for genomic medicine?

Genotype-phenotype databases: challenges and solutions for the post-genomic era.

Geographical structure and differential natural selection among North European populations

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

Identity in research infrastructure and scientific communication: Report from the 1st IRISC workshop, Helsinki Sep 12-13, 2011

NordicDB: a Nordic pool and portal for genome-wide control data

Observ-OM and Observ-TAB: Universal syntax solutions for the integration, search, and exchange of phenotype and genotype information

Paradigm shifts in the approaches for gene annotation

The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.

The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button

The federated database--a basis for biobank-based post-genome studies, integrating phenome and genome data from 600,000 twin pairs in Europe

The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation

VarioML framework for comprehensive variation data representation and exchange