Demo Data from VLDB 2026 / reviewers in the wild / expert
Joffrey Fitz
dblp:79/3552
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2012
0000-0002-1374-3538ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
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 7 heaviest of 8, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
genotyping |
0.1 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Bioinformatics and computational biology › gene expression analysis › gene expression classification
marker gene selection |
0.1 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Bioinformatics and computational biology
sequence analysis |
0.1 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Bioinformatics and computational biology › genomics › computational genomics
SNP detection |
0.1 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Bioinformatics and computational biology › genomics
plant genomics |
0.0 | 1 | 2012 | 1001 Proteomes: a functional proteomics portal for the analysis of Arabidopsis thaliana accessions · Bioinform. 2012 |
Bioinformatics and computational biology
biological database |
0.0 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Bioinformatics and computational biology › sequence analysis › database search
sequence retrieval |
0.0 | 1 | 2007 | MSQT for choosing SNP assays from multiple DNA alignments · Bioinform. 2007 |
Methods — techniques the papers use, named apart from their topics
phosphoproteomics · 0.1nonsynonymous SNP analysis · 0.1multiple sequence alignment · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2012 | 1001 Proteomes: a functional proteomics portal for the analysis of Arabidopsis thaliana accessionsabstractMOTIVATION: The sequencing of over a thousand natural strains of the model plant Arabidopsis thaliana is producing unparalleled information at the genetic level for plant researchers. To enable the rapid exploitation of these data for functional proteomics studies, we have created a resource for the visualization of protein information and proteomic datasets for sequenced natural strains of A. thaliana. RESULTS: The 1001 Proteomes portal can be used to visualize amino acid substitutions or non-synonymous single-nucleotide polymorphisms in individual proteins of A. thaliana based on the reference genome Col-0. We have used the available processed sequence information to analyze the conservation of known residues subject to protein phosphorylation among these natural strains. The substitution of amino acids in A. thaliana natural strains is heavily constrained and is likely a result of the conservation of functional attributes within proteins. At a practical level, we demonstrate that this information can be used to clarify ambiguously defined phosphorylation sites from phosphoproteomic studies. Protein sets of available natural variants are available for download to enable proteomic studies on these accessions. Together this information can be used to uncover the possible roles of specific amino acids in determining the structure and function of proteins in the model plant A. thaliana. An online portal to enable the community to exploit these data can be accessed at http://1001proteomes.masc-proteomics.org/ Hiren J. Joshi, Katy M. Christiansen, Joffrey Fitz, Anna Lipzen, Joel Martin, A. Michelle Smith-Moritz, Len A. Pennacchio, Wendy S. Schackwitz, Detlef Weigel, Joshua L. Heazlewood |
Bioinform. | 3 |
| 2007 | MSQT for choosing SNP assays from multiple DNA alignmentsabstractMOTIVATION: One challenging aspect of genotyping and association mapping projects is often the identification of markers that are informative between groups of individuals and to convert these into genotyping assays. RESULTS: The Multiple SNP Query Tool (MSQT) extracts SNP information from multiple sequence alignments, stores it in a database, provides a web interface to query the database and outputs SNP information in a format directly applicable for SNP-assay design. MSQT was applied to Arabidopsis thaliana sequence data to develop SNP genotyping assays that distinguish a recurrent parent (Col-0) from five other strains. SNPs with intermediate allele frequencies were also identified and developed into markers suitable for efficient genetic mapping among random pairs of wild strains. AVAILABILITY: The source code for MSQT is available at http://msqt.weigelworld.org, together with an online instance of MSQT containing data on 1214 sequenced fragments from 96 ecotypes (wild inbred strains) of the reference plant A. thaliana. All SNP genotyping assays are available in several formats for broad community use. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Norman Warthmann, Joffrey Fitz, Detlef Weigel |
Bioinform. | 2 |