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Remco Loos

dblp:08/3689 · DBLP profile ↗
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13ranked-venue papers
9as first author
1since 2021 · last 2021
0000-0002-9850-6821ORCID · verified

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

Theory of computation · 9 · 8 first-authorApplied, interdisciplinary, general and emerging computing · 3 · 1 since 2021Artificial intelligence and machine learning · 1 · 1 first-author

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
2 papers
Bioinformatics and computational biology · 77% Medical and health informatics · 23%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › epigenomics
chromatin conformation
0.512021
iNucs: inter-nucleosome interactions · Bioinform. 2021
Bioinformatics and computational biology
biomarker discovery
0.412019
DECO: decompose heterogeneous population cohorts for patient stratification and discovery of sample biomarkers using omic data profiling · Bioinform. 2019
Bioinformatics and computational biology
omics data analysis
0.412019
DECO: decompose heterogeneous population cohorts for patient stratification and discovery of sample biomarkers using omic data profiling · Bioinform. 2019
Medical and health informatics › precision medicine
patient stratification
0.412019
DECO: decompose heterogeneous population cohorts for patient stratification and discovery of sample biomarkers using omic data profiling · Bioinform. 2019

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

python · 0.5differential analysis · 0.4correspondence analysis · 0.4
YearPublicationVenuePosition
2021 iNucs: inter-nucleosome interactions
abstract
MOTIVATION: Deciphering nucleosome-nucleosome interactions is an important step toward mesoscale description of chromatin organization but computational tools to perform such analyses are not publicly available. RESULTS: We developed iNucs, a user-friendly and efficient Python-based bioinformatics tool to compute and visualize nucleosome-resolved interactions using standard pairs format input generated from pairtools. AVAILABILITYAND IMPLEMENTATION: https://github.com/Karimi-Lab/inucs/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Mehrdad Oveisi, Manu Shukla, Nogayhan Seymen, Masae Ohno, Yuichi Taniguchi, Sunil Nahata, Remco Loos, Ghulam J. Mufti, Robin C. Allshire, Stefan Dimitrov, Mohammad M. Karimi
Bioinform.7
2019 DECO: decompose heterogeneous population cohorts for patient stratification and discovery of sample biomarkers using omic data profiling
abstract
MOTIVATION: Patient and sample diversity is one of the main challenges when dealing with clinical cohorts in biomedical genomics studies. During last decade, several methods have been developed to identify biomarkers assigned to specific individuals or subtypes of samples. However, current methods still fail to discover markers in complex scenarios where heterogeneity or hidden phenotypical factors are present. Here, we propose a method to analyze and understand heterogeneous data avoiding classical normalization approaches of reducing or removing variation. RESULTS: DEcomposing heterogeneous Cohorts using Omic data profiling (DECO) is a method to find significant association among biological features (biomarkers) and samples (individuals) analyzing large-scale omic data. The method identifies and categorizes biomarkers of specific phenotypic conditions based on a recurrent differential analysis integrated with a non-symmetrical correspondence analysis. DECO integrates both omic data dispersion and predictor-response relationship from non-symmetrical correspondence analysis in a unique statistic (called h-statistic), allowing the identification of closely related sample categories within complex cohorts. The performance is demonstrated using simulated data and five experimental transcriptomic datasets, and comparing to seven other methods. We show DECO greatly enhances the discovery and subtle identification of biomarkers, making it especially suited for deep and accurate patient stratification. AVAILABILITY AND IMPLEMENTATION: DECO is freely available as an R package (including a practical vignette) at Bioconductor repository (http://bioconductor.org/packages/deco/). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Francisco J. Campos-Laborie, Alberto Risueño, M. Ortiz-Estévez, B. Rosón-Burgo, Conrad Droste, Celia Fontanillo, Remco Loos, Jose Manuel Sánchez-Santos, Matthew W. B. Trotter, Javier De Las Rivas
Bioinform.7
2013 Next-generation sequencing: a challenge to meet the increasing demand for training workshops in Australia
abstract
The widespread adoption of high-throughput next-generation sequencing (NGS) technology among the Australian life science research community is highlighting an urgent need to up-skill biologists in tools required for handling and analysing their NGS data. There is currently a shortage of cutting-edge bioinformatics training courses in Australia as a consequence of a scarcity of skilled trainers with time and funding to develop and deliver training courses. To address this, a consortium of Australian research organizations, including Bioplatforms Australia, the Commonwealth Scientific and Industrial Research Organisation and the Australian Bioinformatics Network, have been collaborating with EMBL-EBI training team. A group of Australian bioinformaticians attended the train-the-trainer workshop to improve training skills in developing and delivering bioinformatics workshop curriculum. A 2-day NGS workshop was jointly developed to provide hands-on knowledge and understanding of typical NGS data analysis workflows. The road show-style workshop was successfully delivered at five geographically distant venues in Australia using the newly established Australian NeCTAR Research Cloud. We highlight the challenges we had to overcome at different stages from design to delivery, including the establishment of an Australian bioinformatics training network and the computing infrastructure and resource development. A virtual machine image, workshop materials and scripts for configuring a machine with workshop contents have all been made available under a Creative Commons Attribution 3.0 Unported License. This means participants continue to have convenient access to an environment they had become familiar and bioinformatics trainers are able to access and reuse these resources.
Nathan S. Watson-Haigh, Catherine A. Shang, Matthias Haimel, Myrto Kostadima, Remco Loos, Nandan Deshpande, Konsta Duesing, Annette McGrath, Sean McWilliam, Simon Michnowicz, Paula Moolhuijzen, Steve Quenette, Jerico Revote, Sonika Tyagi, Maria Victoria Schneider
Briefings Bioinform.5
2010 Small universal accepting hybrid networks of evolutionary processors
Remco Loos, Florin Manea, Victor Mitrana
Acta Informatica1
2010 Time and Space Complexity for Splicing Systems
Remco Loos, Mitsunori Ogihara
Theory Comput. Syst.1
2009 On small, reduced, and fast universal accepting networks of splicing processors
Remco Loos, Florin Manea, Victor Mitrana
Theor. Comput. Sci.1
2008 Computational Efficiency of Intermolecular Gene Assembly
Tseren-Onolt Ishdorj, Remco Loos, Ion Petre
Fundam. Informaticae2
2008 1st International Conference on Language and Automata Theory and Applications (LATA 2007)
Remco Loos, Carlos Martín-Vide
Inf. Comput.1
2007 On Accepting Networks of Splicing Processors of Size 3
Remco Loos
CiE1
2007 Complexity Theory for Splicing Systems
Remco Loos, Mitsunori Ogihara
Developments in Language Theory1
2007 Complexity theory for splicing systems
Remco Loos, Mitsunori Ogihara
Theor. Comput. Sci.1
2006 Solving SAT and HPP with Accepting Splicing Systems
Remco Loos, Carlos Martín-Vide, Victor Mitrana
PPSN1
2006 An alternative definition of splicing
Remco Loos
Theor. Comput. Sci.1