Demo Data from VLDB 2026 / reviewers in the wild / expert
Caroline Costedoat
dblp:27/7969
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2010
0000-0002-1848-6366ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
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 › 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
sequence similarity estimation · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 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. | 2 |