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Clemens R. Scherzer

dblp:339/8523 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2021
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 1 · 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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › functional genomics
eQTL mapping
0.512021
powerEQTL: an R package and shiny application for sample size and power calculation of bulk tissue and single-cell eQTL analysis · Bioinform. 2021
Bioinformatics and computational biology
genomics
0.512021
powerEQTL: an R package and shiny application for sample size and power calculation of bulk tissue and single-cell eQTL analysis · Bioinform. 2021
Bioinformatics and computational biology › single-cell analysis
single-cell RNA sequencing
0.512021
powerEQTL: an R package and shiny application for sample size and power calculation of bulk tissue and single-cell eQTL analysis · Bioinform. 2021

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

statistical power analysis · 0.5
YearPublicationVenuePosition
2021 powerEQTL: an R package and shiny application for sample size and power calculation of bulk tissue and single-cell eQTL analysis
abstract
SUMMARY: Genome-wide association studies (GWAS) have revealed thousands of genetic loci for common diseases. One of the main challenges in the post-GWAS era is to understand the causality of the genetic variants. Expression quantitative trait locus (eQTL) analysis is an effective way to address this question by examining the relationship between gene expression and genetic variation in a sufficiently powered cohort. However, it is frequently a challenge to determine the sample size at which a variant with a specific allele frequency will be detected to associate with gene expression with sufficient power. This is a particularly difficult task for single-cell RNAseq studies. Therefore, a user-friendly tool to estimate statistical power for eQTL analyses in both bulk tissue and single-cell data is needed. Here, we presented an R package called powerEQTL with flexible functions to estimate power, minimal sample size or detectable minor allele frequency for both bulk tissue and single-cell eQTL analysis. A user-friendly, program-free web application is also provided, allowing users to calculate and visualize the parameters interactively. AVAILABILITY AND IMPLEMENTATION: The powerEQTL R package source code and online tutorial are freely available at CRAN: https://cran.r-project.org/web/packages/powerEQTL/. The R shiny application is publicly hosted at https://bwhbioinfo.shinyapps.io/powerEQTL/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Xianjun Dong, Xiaoqi Li 0018, Tzuu-Wang Chang, Clemens R. Scherzer, Scott T. Weiss, Weiliang Qiu
Bioinform.4