Lista de obras -

A mathematical approach to the analysis of multiplex DNA profiles

artículo científico publicado en 2010

A mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee

artículo científico publicado en 2013

A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

An open resource for accurately benchmarking small variant and reference calls

scientific article published on 01 April 2019

Assessing and managing risk when sharing aggregate genetic variant data

artículo científico publicado en 2011

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

artículo científico publicado en 2022

Author Correction: A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

Characterizing genetic variants for clinical action

artículo científico publicado en 2014

ClinGen--the Clinical Genome Resource

artículo científico publicado en 2015

Completing the map of human genetic variation

artículo científico publicado en 2007

Consent Codes: Upholding Standard Data Use Conditions

artículo científico publicado en 2016

Data use under the NIH GWAS data sharing policy and future directions

artículo científico publicado en 2014

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2012

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2011

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2010

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2006

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2009

Database resources of the National Center for Biotechnology Information

artículo científico publicado en 2020

Databases in Human and Medical Genetics

article

Epidemiology. DNA identifications after the 9/11 World Trade Center attack

artículo científico publicado en 2005

Extensive sequencing of seven human genomes to characterize benchmark reference materials

artículo científico publicado en 2016

Federated discovery and sharing of genomic data using Beacons

artículo científico publicado en 2019

GenBank

artículo científico publicado en 2020

GenBank

artículo científico

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

High-coverage, long-read sequencing of Han Chinese trio reference samples.

artículo científico publicado en 2019

Indexing pharmacogenetic knowledge on the World Wide Web.

artículo científico publicado en 2003

Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

artículo científico publicado en 2005

Integrative annotation of 21,037 human genes validated by full-length cDNA clones

artículo científico publicado en 2004

Mitochondrial DNA and Y chromosome diversity and the peopling of the Americas: evolutionary and demographic evidence

artículo científico

New approaches to dating suggest a recent age for the human mtDNA ancestor

artículo científico publicado el 29 de agosto de 1992

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

artículo científico publicado en 2013

Publisher Correction: Federated discovery and sharing of genomic data using Beacons

scientific article published on 01 April 2019

Quickly identifying identical and closely related subjects in large databases using genotype data

artículo científico publicado en 2017

Recommendations of the 2006 Human Variome Project meeting

artículo científico publicado en 2007

Registered access: authorizing data access

artículo científico publicado en 2018

Sequence variations in the public human genome data reflect a bottlenecked population history

artículo científico publicado en 2002

Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm

artículo científico publicado en 2009

The 1000 Genomes Project: data management and community access

artículo científico publicado en 2012

The NCBI dbGaP database of genotypes and phenotypes

artículo científico publicado en 2007

The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations

artículo científico publicado en 2004

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data

artículo científico publicado en 2016

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

artículo científico publicado en 2021

Lista de obras de

A mathematical approach to the analysis of multiplex DNA profiles

A mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee

A robust benchmark for detection of germline large deletions and insertions

A second generation human haplotype map of over 3.1 million SNPs

An open resource for accurately benchmarking small variant and reference calls

Assessing and managing risk when sharing aggregate genetic variant data

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

Author Correction: A robust benchmark for detection of germline large deletions and insertions

Characterizing genetic variants for clinical action

ClinGen--the Clinical Genome Resource

Completing the map of human genetic variation

Consent Codes: Upholding Standard Data Use Conditions

Data use under the NIH GWAS data sharing policy and future directions

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Databases in Human and Medical Genetics

Epidemiology. DNA identifications after the 9/11 World Trade Center attack

Extensive sequencing of seven human genomes to characterize benchmark reference materials

Federated discovery and sharing of genomic data using Beacons

GenBank

GenBank

Genome-wide detection and characterization of positive selection in human populations

High-coverage, long-read sequencing of Han Chinese trio reference samples.

Indexing pharmacogenetic knowledge on the World Wide Web.

Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

Integrative annotation of 21,037 human genes validated by full-length cDNA clones

Mitochondrial DNA and Y chromosome diversity and the peopling of the Americas: evolutionary and demographic evidence

New approaches to dating suggest a recent age for the human mtDNA ancestor

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

Publisher Correction: Federated discovery and sharing of genomic data using Beacons

Quickly identifying identical and closely related subjects in large databases using genotype data

Recommendations of the 2006 Human Variome Project meeting

Registered access: authorizing data access

Sequence variations in the public human genome data reflect a bottlenecked population history

Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm

The 1000 Genomes Project: data management and community access

The NCBI dbGaP database of genotypes and phenotypes

The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing