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Now showing items 1-10 of 27
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2009)
Background: Large multigene sequence alignments have over recent years been increasingly employed for phylogenomic reconstruction of the eukaryote tree of life. Such supermatrices of sequence data are preferred over single ...
(Chapter / Bokkapittel / AcceptedVersion; Peer reviewed, 2013)
This paper documents ongoing work within the Norwegian CLARINO project on building a Language Analysis Portal (LAP). The portal will provide an intuitive and easily accessible web interface to a centralized repository of ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2015)
Genotyping chips for rare and low-frequent variants have recently gained popularity with the introduction of exome chips, but the utility of these chips remains unclear. These chips were designed using exome sequencing ...
(Chapter / Bokkapittel / AcceptedVersion; Peer reviewed, 2013)
This demonstration presents a first operable pilot of the Language Analysis Portal (LAP), an ongoing project within the Norwegian CLARINO initiative that aims at providing easy access to Language Technology (LT) tools ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2011)
Background:The implementation of high throughput sequencing for exploring biodiversity poses high demands on bioinformatics applications for automated data processing. Here we introduce CLOTU, an online and open access ...
(Book / Bok / PublishedVersion, 2007)
I artikkelsamlingen kan du lese om pedagogiske endringer i krysningspunktet mellom teknologi, organisering og læring. Du finner artikler fra en rekke ulike fagmiljøer som beskriver prosjekter av mange ulike slag. Erfaringene ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2018)
The Norwegian e-Infrastructure for Life Sciences (NeLS) has been developed by ELIXIR Norway to provide its users with a system enabling data storage, sharing, and analysis in a project-oriented fashion. The system is ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2020)
Abstract Advances in next-generation sequencing technology have enabled whole genome sequencing (WGS) to be widely used for identification of causal variants in a spectrum of genetic-related disorders, and provided new ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2022)
Abstract The heredity of the malignant blood disorders, leukemias, lymphomas and myeloma, has so far been largely unknown. The present study comprises genealogical investigations of one hundred and twelve Scandinavian ...
(Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2022)
BAKGRUNN
Histopatologisk vurdering av melanom og andre melanocytære hudlesjoner kan være vanskelig, og kan variere mellom patologer.
MATERIALE OG METODE
Histopatologiske snitt av 196 melanocytære hudlesjoner fra ...