Demo Data from VLDB 2026 / reviewers in the wild / expert
Emese Meglécz
dblp:28/7971
· DBLP profile ↗
2ranked-venue papers
2as first author
0since 2021 · last 2011
0000-0001-7547-4858ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 2 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 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
genotyping |
0.1 | 1 | 2011 | SESAME (SEquence Sorter & AMplicon Explorer): genotyping based on high-throughput multiplex amplicon sequencing · Bioinform. 2011 |
Bioinformatics and computational biology › genomics
primer design |
0.1 | 1 | 2010 | QDD: a user-friendly program to select microsatellite markers and design primers from large sequencing projects · Bioinform. 2010 |
Bioinformatics and computational biology › statistical genetics › genotype calling
allele calling |
0.0 | 1 | 2011 | SESAME (SEquence Sorter & AMplicon Explorer): genotyping based on high-throughput multiplex amplicon sequencing · Bioinform. 2011 |
Bioinformatics and computational biology › sequence analysis › sequencing data processing
high-throughput sequencing data processing |
0.0 | 1 | 2010 | QDD: a user-friendly program to select microsatellite markers and design primers from large sequencing projects · Bioinform. 2010 |
Methods — techniques the papers use, named apart from their topics
read assignment · 0.1allele validation · 0.1sequence similarity estimation · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2011 | SESAME (SEquence Sorter & AMplicon Explorer): genotyping based on high-throughput multiplex amplicon sequencingabstractSUMMARY: Characterizing genetic diversity through genotyping short amplicons is central to evolutionary biology. Next-generation sequencing (NGS) technologies changed the scale at which these type of data are acquired. SESAME is a web application package that assists genotyping of multiplexed individuals for several markers based on NGS amplicon sequencing. It automatically assigns reads to loci and individuals, corrects reads if standard samples are available and provides an intuitive graphical user interface (GUI) for allele validation based on the sequences and associated decision-making tools. The aim of SESAME is to help allele identification among a large number of sequences. AVAILABILITY: SESAME and its documentation are freely available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported Licence for Windows and Linux from http://www1.montpellier.inra.fr/CBGP/NGS/ or http://tinyurl.com/ngs-sesame. Emese Meglécz, Sylvain Piry, Erick Desmarais, Maxime Galan, André Gilles, Emmanuel Guivier, Nicolas Pech, Jean-François Martin |
Bioinform. | 1 |
| 2010 | QDD: a user-friendly program to select microsatellite markers and design primers from large sequencing projectsabstractSUMMARY: QDD is an open access program providing a user-friendly tool for microsatellite detection and primer design from large sets of DNA sequences. The program is designed to deal with all steps of treatment of raw sequences obtained from pyrosequencing of enriched DNA libraries, but it is also applicable to data obtained through other sequencing methods, using FASTA files as input. The following tasks are completed by QDD: tag sorting, adapter/vector removal, elimination of redundant sequences, detection of possible genomic multicopies (duplicated loci or transposable elements), stringent selection of target microsatellites and customizable primer design. It can treat up to one million sequences of a few hundred base pairs in the tag-sorting step, and up to 50,000 sequences in a single input file for the steps involving estimation of sequence similarity. AVAILABILITY: QDD is freely available under the GPL licence for Windows and Linux from the following web site: http://www.univ-provence.fr/gsite/Local/egee/dir/meglecz/QDD.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Emese Meglécz, Caroline Costedoat, Vincent Dubut, André Gilles, Thibaut Malausa, Nicolas Pech, Jean-François Martin |
Bioinform. | 1 |