Demo Data from EDBT 2026 / reviewers in the wild / expert
Gebhard F. X. Schertler
dblp:28/8711
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2010
0000-0002-5846-6810ORCID · 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 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › multiple sequence alignment
multiple sequence alignment analysis |
0.1 | 1 | 2010 | Spial: analysis of subtype-specific features in multiple sequence alignments of proteins · Bioinform. 2010 |
Bioinformatics and computational biology
protein sequence analysis |
0.1 | 1 | 2010 | Spial: analysis of subtype-specific features in multiple sequence alignments of proteins · Bioinform. 2010 |
Methods — techniques the papers use, named apart from their topics
sequence logo visualization · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2010 | Spial: analysis of subtype-specific features in multiple sequence alignments of proteinsabstractMOTIVATION: Spial (Specificity in alignments) is a tool for the comparative analysis of two alignments of evolutionarily related sequences that differ in their function, such as two receptor subtypes. It highlights functionally important residues that are either specific to one of the two alignments or conserved across both alignments. It permits visualization of this information in three complementary ways: by colour-coding alignment positions, by sequence logos and optionally by colour-coding the residues of a protein structure provided by the user. This can aid in the detection of residues that are involved in the subtype-specific interaction with a ligand, other proteins or nucleic acids. Spial may also be used to detect residues that may be post-translationally modified in one of the two sets of sequences. AVAILABILITY: http://www.mrc-lmb.cam.ac.uk/genomes/spial/; supplementary information is available at http://www.mrc-lmb.cam.ac.uk/genomes/spial/help.html. Arthur Wuster, A. J. Venkatakrishnan, Gebhard F. X. Schertler, M. Madan Babu |
Bioinform. | 3 |