Andrej-Nikolai Spiess

dblp:08/5395 · DBLP profile ↗
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3ranked-venue papers
1as first author
0since 2021 · last 2017
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 3 · 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 · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
nucleic acid quantification
0.312017
Enabling reproducible real-time quantitative PCR research: the RDML package · Bioinform. 2017
Bioinformatics and computational biology
gene expression analysis
0.112008
qpcR: an R package for sigmoidal model selection in quantitative real-time polymerase chain reaction analysis · Bioinform. 2008
Bioinformatics and computational biology › gene expression analysis › gene expression quantification
qPCR data analysis
0.112008
qpcR: an R package for sigmoidal model selection in quantitative real-time polymerase chain reaction analysis · Bioinform. 2008

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

graphical user interface · 0.3data format conversion · 0.3goodness-of-fit statistics · 0.1
YearPublicationVenuePosition
2017 Enabling reproducible real-time quantitative PCR research: the RDML package
abstract
MOTIVATION: Reproducibility, a cornerstone of research, requires defined data formats, which include the setup and output of experiments. The real-time PCR data markup language (RDML) is a recommended standard of the minimum information for publication of quantitative real-time PCR experiments guidelines. Despite the popularity of the RDML format for analysis of quantitative PCR data, handling of RDML files is not yet widely supported in all PCR curve analysis softwares. RESULTS: This study describes the open-source RDML package for the statistical computing language R. RDML is compatible with RDML versions ≤ 1.2 and provides functionality to (i) import RDML data; (ii) extract sample information (e.g. targets and concentration); (iii) transform data to various formats of the R environment; (iv) generate human-readable run summaries; and (v) to create RDML files from user data. In addition, RDML offers a graphical user interface to read, edit and create RDML files. AVAILABILITY AND IMPLEMENTATION: https://cran.r-project.org/package=RDML. rdmlEdit server http://shtest.evrogen.net/rdmlEdit/. Documentation: http://kablag.github.io/RDML/. CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Stefan Rödiger, Michal Burdukiewicz, Andrej-Nikolai Spiess, Konstantin Blagodatskikh
Bioinform.3
2008 qpcR: an R package for sigmoidal model selection in quantitative real-time polymerase chain reaction analysis
abstract
UNLABELLED: The qpcR library is an add-on to the free R statistical environment performing sigmoidal model selection in real-time quantitative polymerase chain reaction (PCR) data analysis. Additionally, the package implements the most commonly used algorithms for real-time PCR data analysis and is capable of extensive statistical comparison for the selection and evaluation of the different models based on several measures of goodness of fit. AVAILABILITY: www.dr-spiess.de/qpcR.html. SUPPLEMENTARY INFORMATION: Statistical evaluations of the implemented methods can be found at www.dr-spiess.de under 'Supplemental Data'.
Christian Ritz 0002, Andrej-Nikolai Spiess
Bioinform.2
2008 Highly accurate sigmoidal fitting of real-time PCR data by introducing a parameter for asymmetry
abstract
BACKGROUND: Fitting four-parameter sigmoidal models is one of the methods established in the analysis of quantitative real-time PCR (qPCR) data. We had observed that these models are not optimal in the fitting outcome due to the inherent constraint of symmetry around the point of inflection. Thus, we found it necessary to employ a mathematical algorithm that circumvents this problem and which utilizes an additional parameter for accommodating asymmetrical structures in sigmoidal qPCR data. RESULTS: The four-parameter models were compared to their five-parameter counterparts by means of nested F-tests based on the residual variance, thus acquiring a statistical measure for higher performance. For nearly all qPCR data we examined, five-parameter models resulted in a significantly better fit. Furthermore, accuracy and precision for the estimation of efficiencies and calculation of quantitative ratios were assessed with four independent dilution datasets and compared to the most commonly used quantification methods. It could be shown that the five-parameter model exhibits an accuracy and precision more similar to the non-sigmoidal quantification methods. CONCLUSION: The five-parameter sigmoidal models outperform the established four-parameter model with high statistical significance. The estimation of essential PCR parameters such as PCR efficiency, threshold cycles and initial template fluorescence is more robust and has smaller variance. The model is implemented in the qpcR package for the freely available statistical R environment. The package can be downloaded from the author's homepage.
Andrej-Nikolai Spiess, Caroline Feig, Christian Ritz 0002
BMC Bioinform.1