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Frontiers in Pediatrics|February 24, 2023
Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignanciesTriantafyllia Brozou, Layal Yasin, Danielle Brandes, et al.BMC Medical Informatics and Decision Making|May 26, 2015
ODM2CDA and CDA2ODM: tools to convert documentation forms between EDC and EHR systemsMartin DugasTrials|December 1, 2016
Design of case report forms based on a public metadata registry: re-use of data elements to improve compatibility of dataMartin DugasStudies in Health Technology and Informatics|August 8, 2013
Why we need a large-scale open metadata initiative in health informatics - a vision paper on open data models for clinical phenotypesMartin DugasJournal of Molecular Biology|August 31, 2014
Chromatin dynamics during differentiation of myeloid cellsJörg Schönheit, Achim Leutz, Frank RosenbauerJournal of Pediatric Hematology/Oncology|May 10, 2022
Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their ParentsRabea Wagener, Carolin Walter, Harald M Surowy, et al.The EMBO Journal|August 31, 2016
Myeloid leukemia with transdifferentiation plasticity developing from T-cell progenitorsPia Riemke, Melinda Czeh, Josephine Fischer, et al.Bioinformatics (Oxford, England)|January 19, 2018
VIPER: a web application for rapid expert review of variant callsMarius Wöste, Martin DugasBMC Bioinformatics|August 4, 2022
Cogito: automated and generic comparison of annotated genomic intervalsAnnika Bürger, Martin DugasBriefings in Bioinformatics|May 23, 2015
Robust and exact structural variation detection with paired-end and soft-clipped alignments: SoftSV compared with eight algorithmsChristoph Bartenhagen, Martin DugasPageof 39