Demo Data from EDBT 2026 / reviewers in the wild / expert
Christopher Harrison
dblp:78/1248
· DBLP profile ↗
2ranked-venue papers
1as first author
0since 2021 · last 2019
0000-0002-6735-6920ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Security and privacy · 1 · 1 first-authorApplied, 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 › gene regulation
regulatory genomics |
0.4 | 1 | 2019 | atSNP Search: a web resource for statistically evaluating influence of human genetic variation on transcription factor binding · Bioinform. 2019 |
Bioinformatics and computational biology › gene regulation
regulatory variant interpretation |
0.4 | 1 | 2019 | atSNP Search: a web resource for statistically evaluating influence of human genetic variation on transcription factor binding · Bioinform. 2019 |
Bioinformatics and computational biology › gene regulation
transcription factor binding |
0.4 | 1 | 2019 | atSNP Search: a web resource for statistically evaluating influence of human genetic variation on transcription factor binding · Bioinform. 2019 |
Methods — techniques the papers use, named apart from their topics
statistical significance testing · 0.4
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2019 | atSNP Search: a web resource for statistically evaluating influence of human genetic variation on transcription factor bindingabstractSUMMARY: Understanding the regulatory roles of non-coding genetic variants has become a central goal for interpreting results of genome-wide association studies. The regulatory significance of the variants may be interrogated by assessing their influence on transcription factor binding. We have developed atSNP Search, a comprehensive web database for evaluating motif matches to the human genome with both reference and variant alleles and assessing the overall significance of the variant alterations on the motif matches. Convenient search features, comprehensive search outputs and a useful help menu are key components of atSNP Search. atSNP Search enables convenient interpretation of regulatory variants by statistical significance testing and composite logo plots, which are graphical representations of motif matches with the reference and variant alleles. Existing motif-based regulatory variant discovery tools only consider a limited pool of variants due to storage or other limitations. In contrast, atSNP Search users can test more than 37 billion variant-motif pairs with marginal significance in motif matches or match alteration. Computational evidence from atSNP Search, when combined with experimental validation, may help with the discovery of underlying disease mechanisms. AVAILABILITY AND IMPLEMENTATION: atSNP Search is freely available at http://atsnp.biostat.wisc.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Sunyoung Shin, Rebecca Hudson, Christopher Harrison, Mark Craven, Sündüz Keles |
Bioinform. | 3 |
| 2012 | Constructing a Cloud-Based IDS by Merging VMI with FMAabstractCloud computing has emerged in recent years as a major segment of the IT industry; however, security concerns remain the primary impediment to full-scale adoption. Leveraging properties of virtualization, virtual machine introspection (VMI) has yielded promising research for cloud security yet adoption of these approaches in production environments remains minimal due to a semantic gap: the extraction of high-level knowledge of the guest operating system's state from low-level artifacts collected out-of-VM. Within the field of forensic memory analysis (FMA), a similar semantic gap exists from the reconstruction of physical memory dumps. We implement a production oriented prototype utilizing designs that combines and narrows these semantic gaps in a modular framework to function as an intrusion detection system (IDS) detecting and defeating post-exploitation activity. Christopher Harrison, Devin Cook, Robert McGraw, John A. Hamilton Jr. |
TrustCom | 1 |