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Vered Madar

dblp:50/10819 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2016
0000-0003-2743-6851ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

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 · 73% Computational science and engineering · 27%

Topics — the 2 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Computational science and engineering › data infrastructure
database
0.112012
seeQTL: a searchable database for human eQTLs · Bioinform. 2012
Bioinformatics and computational biology › functional genomics
eQTL mapping
0.112012
seeQTL: a searchable database for human eQTLs · Bioinform. 2012

Methods — techniques the papers use, named apart from their topics

linear step-up procedure · 0.2meta-analysis · 0.1
YearPublicationVenuePosition
2016 FastLSU: a more practical approach for the Benjamini-Hochberg FDR controlling procedure for huge-scale testing problems
abstract
MOTIVATION: We address a common problem in large-scale data analysis, and especially the field of genetics, the huge-scale testing problem, where millions to billions of hypotheses are tested together creating a computational challenge to control the inflation of the false discovery rate. As a solution we propose an alternative algorithm for the famous Linear Step Up procedure of Benjamini and Hochberg. RESULTS: Our algorithm requires linear time and does not require any P-value ordering. It permits separating huge-scale testing problems arbitrarily into computationally feasible sets or chunks Results from the chunks are combined by our algorithm to produce the same results as the controlling procedure on the entire set of tests, thus controlling the global false discovery rate even when P-values are arbitrarily divided. The practical memory usage may also be determined arbitrarily by the size of available memory. AVAILABILITY AND IMPLEMENTATION: R code is provided in the supplementary material. CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Vered Madar, Sandra Batista
Bioinform.1
2012 seeQTL: a searchable database for human eQTLs
abstract
SUMMARY: seeQTL is a comprehensive and versatile eQTL database, including various eQTL studies and a meta-analysis of HapMap eQTL information. The database presents eQTL association results in a convenient browser, using both segmented local-association plots and genome-wide Manhattan plots. AVAILABILITY AND IMPLEMENTATION: seeQTL is freely available for non-commercial use at http://www.bios.unc.edu/research/genomic_software/seeQTL/. CONTACT: [email protected]; [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Andrey A. Shabalin, Shunping Huang, Vered Madar, Yi-Hui Zhou, Wei Wang 0010, Wei Sun 0006, Patrick F. Sullivan, Fred A. Wright
Bioinform.4