Demo Data from VLDB 2026 / reviewers in the wild / expert
Weiqi Tang
dblp:42/7487
· DBLP profile ↗
3ranked-venue papers
1as first author
0since 2021 · last 2020
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 1 first-authorSecurity and privacy · 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
2 papers |
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 › statistical genetics
quantitative trait locus mapping |
0.8 | 2 | 2020 | BRM: a statistical method for QTL mapping based on bulked segregant analysis by deep sequencing · Bioinform. 2020 Estimation of QTL heritability based on pooled sequencing data · Bioinform. 2018 |
Bioinformatics and computational biology › genomics › high-throughput sequencing
pooled sequencing |
0.3 | 1 | 2018 | Estimation of QTL heritability based on pooled sequencing data · Bioinform. 2018 |
Bioinformatics and computational biology › sequence analysis › high-throughput sequencing data analysis
deep sequencing data analysis |
0.1 | 1 | 2020 | BRM: a statistical method for QTL mapping based on bulked segregant analysis by deep sequencing · Bioinform. 2020 |
Bioinformatics and computational biology
genomics |
0.1 | 1 | 2020 | BRM: a statistical method for QTL mapping based on bulked segregant analysis by deep sequencing · Bioinform. 2020 |
Methods — techniques the papers use, named apart from their topics
multiple testing correction · 0.4confidence interval estimation · 0.4block regression · 0.4maximum likelihood estimation · 0.3bulked segregant analysis · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | BRM: a statistical method for QTL mapping based on bulked segregant analysis by deep sequencingabstractMOTIVATION: Bulked segregant analysis by deep sequencing (BSA-seq) has been widely used for quantitative trait locus (QTL) mapping in recent years. A number of different statistical methods for BSA-seq have been proposed. However, determination of significance threshold, the key point for QTL identification, remains to be a problem that has not been well solved due to the difficulty of multiple testing correction. In addition, estimation of the confidence interval is also a problem to be solved. RESULTS: In this paper, we propose a new statistical method for BSA-seq, named Block Regression Mapping (BRM). BRM is robust to sequencing noise and is applicable to the case of low sequencing depth. Significance threshold can be reasonably determined by taking multiple testing correction into account. Meanwhile, the confidence interval of QTL position can also be estimated. AVAILABILITY AND IMPLEMENTATION: The R scripts of our method are open source under GPLv3 license at https://github.com/huanglikun/BRM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Likun Huang, Weiqi Tang, Suhong Bu |
Bioinform. | 2 |
| 2018 | Estimation of QTL heritability based on pooled sequencing dataabstractMotivation: Bulked segregant analysis combined with next generation sequencing has proven to be a simple and efficient approach for fast mapping of quantitative trait loci (QTLs). However, how to estimate the proportion of phenotypic variance explained by a QTL (or termed QTL heritability) in such pooled QTL mapping is an unsolved problem. Results: In this paper, we propose a method called PQHE to estimate QTL heritability using pooled sequencing data obtained under different experimental designs. Simulation studies indicated that our method is correct and feasible. Four practical examples from rice and yeast are demonstrated, each representing a different situation. Availability and implementation: The R scripts of our method are open source under GPLv3 license at http://genetics.fafu.edu.cn/PQHE or https://github.com/biotangweiqi/PQHE. The R scripts require the R package rootSolve. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online. Weiqi Tang, Likun Huang, Suhong Bu, Xuzhang Zhang |
Bioinform. | 1 |
| 2009 | Research on System of Chinese Document Copy DetectionabstractText copying is easy to do but not easy to be detected. Copy detection is a delicate ground. It determines whether a document is copied from others or not. It helps to verify and to detect paper redistribution, thesis plagiarism or copyright violation. A novel method of Chinese text copy detection design and implementation is discussed in this paper, based on theory of mathematical expression of Chinese characters. It can implement the functions include characteristic reconstruction, registration and detection. Experimental results show that the system has the advantages on detecting accuracy and high speed. Yuzhu Cheng, Chunrong Qiu, Weiqi Tang, Wenda Deng |
IAS | 3 |