about
P2579
P279
Sharing research data to improve public healthInitial sequencing and analysis of the human genomeOpen by default: a proposed copyright license and waiver agreement for open access research and data in peer-reviewed journalsDo pressures to publish increase scientists' bias? An empirical support from US States DataThe diploid genome sequence of an individual humanEthical and practical issues associated with aggregating databasesWhy most published research findings are falseResolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysTroubleshooting public data archiving: suggestions to increase participationEmpirical study of data sharing by authors publishing in PLoS journalsHow many scientists fabricate and falsify research? A systematic review and meta-analysis of survey dataOpen clinical trial data for all? A view from regulatorsData cleaning: detecting, diagnosing, and editing data abnormalitiesResearch ethics recommendations for whole-genome research: consensus statementReporting bias in medical research - a narrative reviewThe SAIL Databank: building a national architecture for e-health research and evaluationPreparing raw clinical data for publication: guidance for journal editors, authors, and peer reviewersThe Sequence of the Human GenomeAn integrated map of genetic variation from 1,092 human genomesThe complete genome of an individual by massively parallel DNA sequencingSample, data use and protection in biobanking in Europe: legal issuesA vision for the future of genomics researchDrug development: Raise standards for preclinical cancer researchData sharing: Make outbreak research open accessData Sharing in Historical PerspectiveDeveloping Global Norms for Sharing Data and Results during Public Health EmergenciesSharing Research Data to Improve Public Health: A Funder PerspectiveSelective Publication of Antidepressant Trials and Its Influence on Apparent EfficacyA multidisciplinary approach to honest broker services for tissue banks and clinical data: a pragmatic and practical modelEthical considerations, confidentiality issues, rights of human subjects, and uses of monitoring data in research and regulationPreparing for Responsible Sharing of Clinical Trial DataSharing health data: good intentions are not enoughTowards a data sharing Code of Conduct for international genomic researchTime for fair trade in research dataFalse-Positive Psychology: Undisclosed Flexibility in Data Collection and Analysis Allows Presenting Anything as SignificantAvoiding Data Dumpsters — Toward Equitable and Useful Data SharingWillingness to share research data is related to the strength of the evidence and the quality of reporting of statistical resultsRedefining genomic privacy: trust and empowermentConsiderations for observational research using large data sets in radiation oncologyDigital images are data: and should be treated as such
P921
description
etiko pri dateno
@eo
moral system around systematic collections of information
@en
système moral qui évolue dans la collection systématique de données
@fr
name
data ethics
@en
datena etiko
@eo
etica dei dati
@it
etika data
@id
ètica de dades
@ca
éthique de la donnée
@fr
ética de los datos
@es
type
label
data ethics
@en
datena etiko
@eo
etica dei dati
@it
etika data
@id
ètica de dades
@ca
éthique de la donnée
@fr
ética de los datos
@es
altLabel
datuma etiko
@eo
prefLabel
data ethics
@en
datena etiko
@eo
etica dei dati
@it
etika data
@id
ètica de dades
@ca
éthique de la donnée
@fr
ética de los datos
@es