Demo Data from VLDB 2026 / reviewers in the wild / expert
Michael R. Stratton
dblp:53/9423
· DBLP profile ↗
2ranked-venue papers
0as first author
1since 2021 · last 2023
0000-0001-6035-153XORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 since 2021
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 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
cancer genomics |
0.7 | 2 | 2023 | Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment · Bioinform. 2023 AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes · Bioinform. 2007 |
Bioinformatics and computational biology › cancer genomics
mutational signature analysis |
0.7 | 1 | 2023 | Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment · Bioinform. 2023 |
Bioinformatics and computational biology › cancer genomics › somatic mutation analysis
somatic variant detection |
0.1 | 1 | 2007 | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes · Bioinform. 2007 |
Methods — techniques the papers use, named apart from their topics
sparse regression · 0.7non-negative least squares · 0.7forward stagewise algorithm · 0.7mutation detection algorithm · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2023 | Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignmentabstractMOTIVATION: Analysis of mutational signatures is a powerful approach for understanding the mutagenic processes that have shaped the evolution of a cancer genome. To evaluate the mutational signatures operative in a cancer genome, one first needs to quantify their activities by estimating the number of mutations imprinted by each signature. RESULTS: Here we present SigProfilerAssignment, a desktop and an online computational framework for assigning all types of mutational signatures to individual samples. SigProfilerAssignment is the first tool that allows both analysis of copy-number signatures and probabilistic assignment of signatures to individual somatic mutations. As its computational engine, the tool uses a custom implementation of the forward stagewise algorithm for sparse regression and nonnegative least squares for numerical optimization. Analysis of 2700 synthetic cancer genomes with and without noise demonstrates that SigProfilerAssignment outperforms four commonly used approaches for assigning mutational signatures. AVAILABILITY AND IMPLEMENTATION: SigProfilerAssignment is available under the BSD 2-clause license at https://github.com/AlexandrovLab/SigProfilerAssignment with a web implementation at https://cancer.sanger.ac.uk/signatures/assignment/. Marcos Díaz-Gay, Raviteja Vangara, Mark Barnes, Xi Wang 0042, S. M. Ashiqul Islam, Ian Vermes, Stephen Duke, Nithish Bharadhwaj Narasimman, Zichen Jiang, Sarah J. Moody, Sergey Senkin, Paul Brennan, Michael R. Stratton, Ludmil B. Alexandrov |
Bioinform. | 14 |
| 2007 | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomesabstractUNLABELLED: The undertaking of large-scale DNA sequencing screens for somatic variants in human cancers requires accurate and rapid processing of traces for variants. Due to their often aneuploid nature and admixed normal tissue, heterozygous variants found in primary cancers are often subtle and difficult to detect. To address these issues, we have developed a mutation detection algorithm, AutoCSA, specifically optimized for the high throughput screening of cancer samples. AVAILABILITY: http://www.sanger.ac.uk/genetics/CGP/Software/AutoCSA. Ed Dicks, Jon W. Teague, Philip Stephens, Keiran Raine, Andy Yates, C. Mattocks, P. Tarpey, Adam P. Butler, Andrew Menzies, Andrew M. Jenkinson, Helen Davies, Sarah Edkins, Simon A. Forbes, Kristian A. Gray, Christopher Greenman, Rebecca Shepherd, Michael R. Stratton, P. Andrew Futreal, Richard Wooster |
Bioinform. | 18 |