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Carlos Morcillo-Suarez

dblp:95/56 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2011
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2 · 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 · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome-wide association study
0.112011
Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management · Bioinform. 2011
Bioinformatics and computational biology › statistical genetics
single nucleotide polymorphism analysis
0.112011
Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management · Bioinform. 2011
Bioinformatics and computational biology › statistical genetics › single nucleotide polymorphism analysis
SNP association analysis
0.112008
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data · Bioinform. 2008
Bioinformatics and computational biology › biostatistics › statistical bioinformatics
statistical genomics
0.112008
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data · Bioinform. 2008
Bioinformatics and computational biology
genetic epidemiology
0.012008
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data · Bioinform. 2008

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

database technology · 0.1quality control · 0.1association testing · 0.1
YearPublicationVenuePosition
2011 Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management
abstract
MOTIVATION: Genome-wide association studies (GWAS) based on single nucleotide polymorphism (SNP) arrays are the most widely used approach to detect loci associated to human traits. Due to the complexity of the methods and software packages available, each with its particular format requiring intricate management workflows, the analysis of GWAS usually confronts scientists with steep learning curves. Indeed, the wide variety of tools makes the parsing and manipulation of data the most time consuming and error prone part of a study. To help resolve these issues, we present GWASpi, a user-friendly, multiplatform, desktop-able application for the management and analysis of GWAS data, with a novel approach on database technologies to leverage the most out of commonly available desktop hardware. GWASpi aims to be a start-to-finish GWAS management application, from raw data to results, containing the most common analysis tools. As a result, GWASpi is easy to use and reduces in up to two orders of magnitude the time needed to perform the fundamental steps of a GWAS. AVAILABILITY: Freely available on the web at http://www.gwaspi.org. Implemented in Java, Apache-Derby and NetCDF-3, with all major operating systems supported. CONTACT: [email protected]; [email protected].
Fernando Muñiz-Fernandez, Angel Carreño-Torres, Carlos Morcillo-Suarez, Arcadi Navarro
Bioinform.3
2008 SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data
abstract
UNLABELLED: Single nucleotide polymorphisms (SNPs) are the most widely used marker in studies to assess associations between genetic variants and complex traits or diseases. They are also becoming increasingly important in the study of the evolution and history of humans and other species. The analysis and processing of SNPs obtained thanks to high-throughput technologies imply the time consuming and costly use of different, complex and usually format-incompatible software. SNPator is a user-friendly web-based SNP data analysis suite that integrates, among many other algorithms, the most common steps of a SNP association study. It frees the user from the need to have large computer facilities and an in depth knowledge of genetic software installation and management. Genotype data is directly read from the output files of the usual genotyping platforms. Phenotypic data on the samples can also be easily uploaded. Many different quality control and analysis procedures can be performed either by using built-in SNPator algorithms or by calling standard genetic software. AVAILABILITY: Access is granted from the SNPator webpage http://www.snpator.org.
Carlos Morcillo-Suarez, Josep Alegre, Ricardo Sangros, Elodie Gazave, Rafael de Cid, Roger Milne, Jorge Amigo, Anna Ferrer-Admetlla, Andrés Moreno-Estrada, Michelle Gardner, Ferran Casals, Anna Pérez-Lezaun, David Comas, Elena Bosch, Francesc Calafell, Jaume Bertranpetit, Arcadi Navarro
Bioinform.1