Groups: Researchers can cluster documents, codes, memos, and networks to use them as filters.Īll these components can be compiled in a project bundle (.atlproj).Networks: They represent relationships between codes, quotations, documents, memos, etc.Memos: Notebooks where researchers write down their thoughts and ideas as they code.Codes: Short phrases or words that describe quotations.Quotations: Selections from your documents that are considered important.ATLAS.ti project components:ĪTLAS.ti projects can have the following main elements: The project files can contain text documents, images, audio recordings, videos, pdf files, geo data, Twitter data, citations from Evernote and reference managers, and survey data. ATLAS.ti handles different types of data that are kept in a project. Description of format OverviewĪltas.ti is a software application that allows researchers to analyze qualitative data in a systematic and transparent way, increasing the validity of results (Friese 2019). Unresolved Issues/Further Questions ĭocumentation of curation process: What do capture from curation process ![]() What to look for to make sure this file meets FAIR principles Resources/Software for viewing or analyzing data Key clarifications to get from researcherĪpplicable metadata standard, core elements and readme requirements These workshops have been generously funded by the Institute of Museum and Library Services # RE-85-18-0040-18. This work was created as part of the “Specialized Data Curation” Workshop #2 held at Johns Hopkins University in Baltimore, MD on April 17-18, 2019. Information about importing projects created in older versions. Added a link to information about QDPX files. Added a section on Human Subjects concerns. Notes about REFI-QDA standard, converting files from different versions, added information about codebooks. Margarita Corral ( updated and summary of changes made result reports, codebook) outside the project? ![]() Is there sensitive information that can compromise human subjects’ rights?Īre there associated data that have been exported (i.e. ATLAS.ti Scientific Software Development GmbH.Ĭan other researchers open the project without the ATLAS.ti?ĭoes the project include metadata/documentation/codebook?Īre there consent forms/participation agreements? hpr6 or hpr7 : Files (ATLAS.ti 6.x and 7.x)ĪTLAS.ti is used for qualitative data analysis in multiple disciplines, especially in the humanities and social science disciplines.ĪTLAS.ti is proprietary software.acb: Formats to transfer/store files (ATLAS.ti 6.x and 7.x) atlpac : File Project/Transfer Bundle (older versions) Patterns of and Experiences with Dysphagia in People with Hypermobile Ehlers Danlos Syndrome (hEDS) With or Without DysautonomiaAuthor: Margarita Corral, Brandeis University ( Contributor: Hannah Hadley, Penn State ( David Fearon, Johns Hopkins, ( Topic Based on analysis of the experiences, signs, symptoms, and factors impacting swallowing in people with EDS, themes and actionable factors will be derived and discussed. ![]() The interviews will be audio/visual recorded, orthographically transcribed, and then analyzed using Atlas.ti 84 Web. We will use a phenomenological qualitative approach, including questionnaires and a semi-structured interview. The purpose of this study is to identify patterns and actionable factors which contribute to dysphagia in people with hEDS with or without comorbid dysautonomia. Our long-term hypothesis is that hEDS’s impact on swallowing is multifaceted and related to both structural and physiological impairments. Despite only one article in the current literature, the prevalence of dysphagia in EDS is not insignificant and warrants further investigation. A Cohort Discovery analysis at Oregon Health & Science University (OHSU) revealed that 14.9% ± 0.3% of patients with an ICD-10 diagnosis of EDS also have an ICD-10 diagnosis of dysphagia in their medical record. However, EDS is associated with symptoms and conditions affecting nearly all body systems, including swallowing (dysphagia). Historically, the musculoskeletal and dermatological manifestations have been emphasized. Ehlers Danlos Syndromes (EDS) are collagen-based hereditary connective tissue disorders characterized by decreased tissue integrity.
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