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Studies in Health Technology and Informatics
|
June 25, 2020
Applying the FAIR Data Principles to the Registry of Vascular Anomalies (VASCA)
Bruna Dos Santos Vieira, Karlijn Groenen, P A C 't Hoen, et al.
Journal of Biomedical Semantics
|
June 19, 2026
FAIR in practice: minimum metadata schema for bioinformatics analytics by machines
Daphne Wijnbergen, Núria Queralt-Rosinach, Valérie Barbié, et al.
BMC Research Notes
|
August 20, 2008
SigWin-detector: a Grid-enabled workflow for discovering enriched windows of genomic features related to DNA sequences
Márcia A Inda, Marinus F van Batenburg, Marco Roos, et al.
Genome Research
|
August 14, 2003
The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes
Rogier Versteeg, Barbera D C van Schaik, Marinus F van Batenburg, et al.
Nucleic Acids Research
|
May 21, 2010
BioCatalogue: a universal catalogue of web services for the life sciences
Jiten Bhagat, Franck Tanoh, Eric Nzuobontane, et al.
Omics : a Journal of Integrative Biology
|
March 27, 2009
The construction of genome-based transcriptional units
Sander R van Hooff, Jan Koster, Tim Hulsen, et al.
BMC Primary Care
|
July 9, 2026
Sustainable implementation of practice-based research networks in primary care: a qualitative process evaluation of the Bavarian Research Practice Network (BayFoNet)
Linda Sanftenberg, Ulrike Stark-Felbinger, Stefanie Eck, et al.
Psychotherapie, Psychosomatik, Medizinische Psychologie
|
March 21, 2015
[Integrated Peer Teaching of Communication and Clinical Skills: How to Train Student Tutors?]
Nadja Ringel, Barbara Maatouk Bürmann, Erika Fellmer-Drueg, et al.
Orphanet Journal of Rare Diseases
|
July 27, 2023
Machine learning in Huntington's disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction
Jasper Ouwerkerk, Stephanie Feleus, Kasper F van der Zwaan, et al.
Human Mutation
|
April 29, 2018
MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases
Gillian S Townend, Friederike Ehrhart, Henk J van Kranen, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 109) with videos related to
Sort By:
Page
of 11
Studies in Health Technology and Informatics
|
June 25, 2020
Applying the FAIR Data Principles to the Registry of Vascular Anomalies (VASCA)
Bruna Dos Santos Vieira, Karlijn Groenen, P A C 't Hoen, et al.
Journal of Biomedical Semantics
|
June 19, 2026
FAIR in practice: minimum metadata schema for bioinformatics analytics by machines
Daphne Wijnbergen, Núria Queralt-Rosinach, Valérie Barbié, et al.
BMC Research Notes
|
August 20, 2008
SigWin-detector: a Grid-enabled workflow for discovering enriched windows of genomic features related to DNA sequences
Márcia A Inda, Marinus F van Batenburg, Marco Roos, et al.
Genome Research
|
August 14, 2003
The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes
Rogier Versteeg, Barbera D C van Schaik, Marinus F van Batenburg, et al.
Nucleic Acids Research
|
May 21, 2010
BioCatalogue: a universal catalogue of web services for the life sciences
Jiten Bhagat, Franck Tanoh, Eric Nzuobontane, et al.
Omics : a Journal of Integrative Biology
|
March 27, 2009
The construction of genome-based transcriptional units
Sander R van Hooff, Jan Koster, Tim Hulsen, et al.
BMC Primary Care
|
July 9, 2026
Sustainable implementation of practice-based research networks in primary care: a qualitative process evaluation of the Bavarian Research Practice Network (BayFoNet)
Linda Sanftenberg, Ulrike Stark-Felbinger, Stefanie Eck, et al.
Psychotherapie, Psychosomatik, Medizinische Psychologie
|
March 21, 2015
[Integrated Peer Teaching of Communication and Clinical Skills: How to Train Student Tutors?]
Nadja Ringel, Barbara Maatouk Bürmann, Erika Fellmer-Drueg, et al.
Orphanet Journal of Rare Diseases
|
July 27, 2023
Machine learning in Huntington's disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction
Jasper Ouwerkerk, Stephanie Feleus, Kasper F van der Zwaan, et al.
Human Mutation
|
April 29, 2018
MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases
Gillian S Townend, Friederike Ehrhart, Henk J van Kranen, et al.
Page
of 11