Demo Data from VLDB 2026 / reviewers in the wild / expert
Eduardo Vilar
dblp:310/6950
· DBLP profile ↗
2ranked-venue papers
0as first author
1since 2021 · last 2022
0000-0001-6404-3761ORCID · 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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › cancer genomics
allelic imbalance detection |
0.2 | 1 | 2016 | Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq · Bioinform. 2016 |
Bioinformatics and computational biology
cancer genomics |
0.2 | 1 | 2016 | Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq · Bioinform. 2016 |
Bioinformatics and computational biology › genomics › next-generation sequencing data analysis
exome sequencing analysis |
0.2 | 1 | 2016 | Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq · Bioinform. 2016 |
Bioinformatics and computational biology › cancer genomics › chromosomal aberration detection
loss of heterozygosity detection |
0.2 | 1 | 2016 | Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq · Bioinform. 2016 |
Methods — techniques the papers use, named apart from their topics
next-generation sequencing · 0.2haplotype-based analysis · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2022 | Sensei: how many samples to tell a change in cell type abundance?abstractCellular heterogeneity underlies cancer evolution and metastasis. Advances in single-cell technologies such as single-cell RNA sequencing and mass cytometry have enabled interrogation of cell type-specific expression profiles and abundance across heterogeneous cancer samples obtained from clinical trials and preclinical studies. However, challenges remain in determining sample sizes needed for ascertaining changes in cell type abundances in a controlled study. To address this statistical challenge, we have developed a new approach, named Sensei, to determine the number of samples and the number of cells that are required to ascertain such changes between two groups of samples in single-cell studies. Sensei expands the t-test and models the cell abundances using a beta-binomial distribution. We evaluate the mathematical accuracy of Sensei and provide practical guidelines on over 20 cell types in over 30 cancer types based on knowledge acquired from the cancer cell atlas (TCGA) and prior single-cell studies. We provide a web application to enable user-friendly study design via https://kchen-lab.github.io/sensei/table_beta.html . Shaoheng Liang, Jason Willis, Jinzhuang Dou, Vakul Mohanty, Yuefan Huang, Eduardo Vilar, Ken Chen 0001 |
BMC Bioinform. | 6 |
| 2016 | Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseqabstractMOTIVATION: The detection of subtle genomic allelic imbalance events has many potential applications. For example, identifying cancer-associated allelic imbalanced regions in low tumor-cellularity samples or in low-proportion tumor subclones can be used for early cancer detection, prognostic assessment and therapeutic selection in cancer patients. We developed hapLOHseq for the detection of subtle allelic imbalance events from next-generation sequencing data. RESULTS: Our method identified events of 10 megabases or greater occurring in as little as 16% of the sample in exome sequencing data (at 80×) and 4% in whole genome sequencing data (at 30×), far exceeding the capabilities of existing software. We also found hapLOHseq to be superior at detecting large chromosomal changes across a series of pancreatic samples from TCGA. AVAILABILITY AND IMPLEMENTATION: hapLOHseq is available at scheet.org/software, distributed under an open source MIT license. CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. F. Anthony San Lucas, Smruthy Sivakumar, Selina Vattathil, Jerry Fowler, Eduardo Vilar, Paul Scheet |
Bioinform. | 5 |