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Miriam L. Gifford

dblp:65/155 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0002-4005-2513ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2

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 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological network › network biology › network inference
causal network inference
0.212014
Correcting for link loss in causal network inference caused by regulator interference · Bioinform. 2014
Bioinformatics and computational biology › biological network › network biology › network inference
gene regulatory network inference
0.212014
Correcting for link loss in causal network inference caused by regulator interference · Bioinform. 2014
Bioinformatics and computational biology › functional genomics
functional enrichment analysis
0.112007
Sungear: interactive visualization and functional analysis of genomic datasets · Bioinform. 2007
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
gene ontology overrepresentation
0.112007
Sungear: interactive visualization and functional analysis of genomic datasets · Bioinform. 2007
Bioinformatics and computational biology › genomics
genome visualization
0.112007
Sungear: interactive visualization and functional analysis of genomic datasets · Bioinform. 2007

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

conditional link probability analysis · 0.2interactive visualization · 0.1
YearPublicationVenuePosition
2014 Correcting for link loss in causal network inference caused by regulator interference
abstract
MOTIVATION: There are a number of algorithms to infer causal regulatory networks from time series (gene expression) data. Here we analyse the phenomena of regulator interference, where regulators with similar dynamics mutually suppress both the probability of regulating a target and the associated link strength; for instance, interference between two identical strong regulators reduces link probabilities by ∼50%. RESULTS: We construct a robust method to define an interference-corrected causal network based on an analysis of the conditional link probabilities that recovers links lost through interference. On a large real network (Streptomyces coelicolor, phosphate depletion), we demonstrate that significant interference can occur between regulators with a correlation as low as 0.865, losing an estimated 34% of links by interference. However, levels of interference cannot be predicted from the correlation between regulators alone and are data specific. Validating against known networks, we show that high numbers of functional links are lost by regulator interference. Performance against other methods on DREAM4 data is excellent. AVAILABILITY AND IMPLEMENTATION: The method is implemented in R and is publicly available as the NIACS package at http://www2.warwick.ac.uk/fac/sci/systemsbiology/research/software.
Christopher A. Penfold, David A. Hodgson, Miriam L. Gifford, Nigel J. Burroughs
Bioinform.4
2007 Sungear: interactive visualization and functional analysis of genomic datasets
abstract
UNLABELLED: Sungear is a software system that supports a rapid, visually interactive and biologist-driven comparison of large datasets. The datasets can come from microarray experiments (e.g. genes induced in each experiment), from comparative genomics (e.g. genes present in each genome) or even from non-biological applications (e.g. demographics or baseball statistics). Sungear represents multiple datasets as vertices in a polygon. Each possible intersection among the sets is represented as a circle inside the polygon. The position of the circle is determined by the position of the vertices represented in the intersection and the area of the circle is determined by the number of elements in the intersection. Sungear shows which Gene Ontology terms are over-represented in a subset of circles or anchors. The intuitive Sungear interface has enabled biologists to determine quickly which dataset or groups of datasets play a role in a biological function of interest. AVAILABILITY: A live online version of Sungear can be found at http://virtualplant-prod.bio.nyu.edu/cgi-bin/sungear/index.cgi
Christopher S. Poultney, Rodrigo A. Gutiérrez, Manpreet S. Katari, Miriam L. Gifford, W. Bradford Paley, Gloria M. Coruzzi, Dennis E. Shasha
Bioinform.4