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Johan Rung

dblp:48/4445 · DBLP profile ↗
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4ranked-venue papers
0as first author
0since 2021 · last 2020
0000-0001-5875-8429ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 4

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
3 papers
Bioinformatics and computational biology · 84% Medical and health informatics · 16%

Topics — the 6 heaviest of 8, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genomics
0.112012
Tools for mapping high-throughput sequencing data · Bioinform. 2012
Bioinformatics and computational biology › genomics
high-throughput sequencing
0.112012
Tools for mapping high-throughput sequencing data · Bioinform. 2012
Bioinformatics and computational biology › sequence analysis
read mapping
0.112012
Tools for mapping high-throughput sequencing data · Bioinform. 2012
Medical and health informatics › biomedical data science
biomedical data management
0.112009
A System for Information Management in BioMedical Studies - SIMBioMS · Bioinform. 2009
Bioinformatics and computational biology
data integration
0.012011
SAIL - a software system for sample and phenotype availability across biobanks and cohorts · Bioinform. 2011
Medical and health informatics › clinical informatics
clinical data management
0.012009
A System for Information Management in BioMedical Studies - SIMBioMS · Bioinform. 2009

Methods — techniques the papers use, named apart from their topics

survey · 0.1logical query expressions · 0.1data import and export · 0.1data archiving · 0.1
YearPublicationVenuePosition
2020 Ten simple rules for annotating sequencing experiments
Irene Stevens, Abdul Kadir Mukarram, Matthias Hörtenhuber, Terrence F. Meehan, Johan Rung, Carsten O. Daub
PLoS Comput. Biol.5
2012 Tools for mapping high-throughput sequencing data
abstract
Abstract Motivation: A ubiquitous and fundamental step in high-throughput sequencing analysis is the alignment (mapping) of the generated reads to a reference sequence. To accomplish this task, numerous software tools have been proposed. Determining the mappers that are most suitable for a specific application is not trivial. Results: This survey focuses on classifying mappers through a wide number of characteristics. The goal is to allow practitioners to compare the mappers more easily and find those that are most suitable for their specific problem. Availability: A regularly updated compendium of mappers can be found at http://wwwdev.ebi.ac.uk/fg/hts_mappers/. Contact: [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
Nuno A. Fonseca, Johan Rung, Alvis Brazma, John C. Marioni
Bioinform.2
2011 SAIL - a software system for sample and phenotype availability across biobanks and cohorts
abstract
Abstract Summary: The Sample avAILability system—SAIL—is a web based application for searching, browsing and annotating biological sample collections or biobank entries. By providing individual-level information on the availability of specific data types (phenotypes, genetic or genomic data) and samples within a collection, rather than the actual measurement data, resource integration can be facilitated. A flexible data structure enables the collection owners to provide descriptive information on their samples using existing or custom vocabularies. Users can query for the available samples by various parameters combining them via logical expressions. The system can be scaled to hold data from millions of samples with thousands of variables. Availability: SAIL is available under Aferro-GPL open source license: https://github.com/sail. Contact: [email protected], [email protected] Supplementary information: Supplementary data are available at Bioinformatics online and from http://www.simbioms.org.
Mikhail Gostev, Julio Fernandez-Banet, Johan Rung, Joern Dietrich, Inga Prokopenko, Samuli Ripatti, Mark I. McCarthy, Alvis Brazma, Maria Krestyaninova
Bioinform.3
2009 A System for Information Management in BioMedical Studies - SIMBioMS
abstract
UNLABELLED: SIMBioMS is a web-based open source software system for managing data and information in biomedical studies. It provides a solution for the collection, storage, management and retrieval of information about research subjects and biomedical samples, as well as experimental data obtained using a range of high-throughput technologies, including gene expression, genotyping, proteomics and metabonomics. The system can easily be customized and has proven to be successful in several large-scale multi-site collaborative projects. It is compatible with emerging functional genomics data standards and provides data import and export in accepted standard formats. Protocols for transferring data to durable archives at the European Bioinformatics Institute have been implemented. AVAILABILITY: The source code, documentation and initialization scripts are available at http://simbioms.org.
Maria Krestyaninova, Andris Zarins, Juris Viksna, Natalja Kurbatova, Peteris Rucevskis, Sudeshna Guha Neogi, Mikhail Gostev, Teemu Perheentupa, Juha Knuuttila, Amy Barrett, Ilkka Lappalainen, Johan Rung, Karlis Podnieks, Ugis Sarkans, Mark I. McCarthy, Alvis Brazma
Bioinform.12