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Christopher M. Ward

dblp:73/10247 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2020
0000-0003-0227-0189ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 1, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis › sequencing data processing
next-generation sequencing quality control
0.412020
ngsReports: a Bioconductor package for managing FastQC reports and other NGS related log files · Bioinform. 2020

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

hierarchical clustering · 0.4
YearPublicationVenuePosition
2020 ngsReports: a Bioconductor package for managing FastQC reports and other NGS related log files
abstract
MOTIVATION: High throughput next generation sequencing (NGS) has become exceedingly cheap, facilitating studies to be undertaken containing large sample numbers. Quality control (QC) is an essential stage during analytic pipelines and the outputs of popular bioinformatics tools such as FastQC and Picard can provide information on individual samples. Although these tools provide considerable power when carrying out QC, large sample numbers can make inspection of all samples and identification of systemic bias a challenge. RESULTS: We present ngsReports, an R package designed for the management and visualization of NGS reports from within an R environment. The available methods allow direct import into R of FastQC reports along with outputs from other tools. Visualization can be carried out across many samples using default, highly customizable plots with options to perform hierarchical clustering to quickly identify outlier libraries. Moreover, these can be displayed in an interactive shiny app or HTML report for ease of analysis. AVAILABILITY AND IMPLEMENTATION: The ngsReports package is available on Bioconductor and the GUI shiny app is available at https://github.com/UofABioinformaticsHub/shinyNgsreports. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Christopher M. Ward, Thu-Hien To, Stephen M. Pederson
Bioinform.1