Demo Data from EDBT 2026 / reviewers in the wild / expert
M. Busch
dblp:47/1417
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 1991
—ORCID · none
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 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › synthetic biology
oligonucleotide design |
0.0 | 1 | 1991 | An improved microcomputer program for finding gene- or gene family-specific oligonucleotides suitable as primers for polymerase chain reactions or as probes · Comput. Appl. Biosci. 1991 |
Bioinformatics and computational biology › sequence analysis
primer and probe design |
0.0 | 1 | 1991 | An improved microcomputer program for finding gene- or gene family-specific oligonucleotides suitable as primers for polymerase chain reactions or as probes · Comput. Appl. Biosci. 1991 |
Bioinformatics and computational biology
sequence analysis |
0.0 | 1 | 1991 | An improved microcomputer program for finding gene- or gene family-specific oligonucleotides suitable as primers for polymerase chain reactions or as probes · Comput. Appl. Biosci. 1991 |
Methods — techniques the papers use, named apart from their topics
sequence scanning · 0.0secondary structure avoidance · 0.0
| Year | Publication | Venue | Position |
|---|---|---|---|
| 1991 | An improved microcomputer program for finding gene- or gene family-specific oligonucleotides suitable as primers for polymerase chain reactions or as probesabstractWe present here an easy-to-use computer program which finds oligonucleotides suitable as primers in polymerase chain reactions (PCR) or as probes for hybridization. In contrast to other programs used for this purpose, the additional advantage of this one is the possibility of directly detecting gene- as well as gene family-specific oligonucleotides. For this purpose, up to 200 different DNA sequences, of maximally 65,000 nucleotides each, can be scanned in a single search to ensure either single or multiple gene binding of the PCR primers or probes. Specific oligonucleotides for genes carrying internal repetitions and for single genes belonging to a set of highly conserved genes can also be detected. Many parameters such as exclusion of simple sequences, which are known to be highly repeated throughout various genomes or regions of stable secondary structures in both primer-primer and primer-template, can be taken into consideration and avoided. Furthermore, the G + C content and the length of the oligonucleotides can be changed in a broad range by the user. K. Lucas, M. Busch, S. Mossinger, J. A. Thompson |
Comput. Appl. Biosci. | 2 |