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Marta Byrska-Bishop

dblp:199/4936 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2023
0000-0002-9118-1032ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
statistical genetics
0.712023
Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics
genetic association study
0.312018
Novel features and enhancements in BioBin, a tool for the biologically inspired binning and association analysis of rare variants · Bioinform. 2018
Bioinformatics and computational biology › statistical genetics
rare variant analysis
0.312018
Novel features and enhancements in BioBin, a tool for the biologically inspired binning and association analysis of rare variants · Bioinform. 2018

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

network analysis · 0.7comorbidity scoring algorithm · 0.7statistical association testing · 0.3binning algorithm · 0.3
YearPublicationVenuePosition
2023 Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
abstract
MOTIVATION: Understanding comorbidity is essential for disease prevention, treatment and prognosis. In particular, insight into which pairs of diseases are likely or unlikely to co-occur may help elucidate the potential relationships between complex diseases. Here, we introduce the use of an inter-disease interactivity network to discover/prioritize comorbidities. Specifically, we determine disease associations by accounting for the direction of effects of genetic components shared between diseases, and categorize those associations as synergistic or antagonistic. We further develop a comorbidity scoring algorithm to predict whether diseases are more or less likely to co-occur in the presence of a given index disease. This algorithm can handle networks that incorporate relationships with opposite signs. RESULTS: We finally investigate inter-disease associations among 427 phenotypes in UK Biobank PheWAS data and predict the priority of comorbid diseases. The predicted comorbidities were verified using the UK Biobank inpatient electronic health records. Our findings demonstrate that considering the interaction of phenotype associations might be helpful in better predicting comorbidity. AVAILABILITY AND IMPLEMENTATION: The source code and data of this study are available at https://github.com/dokyoonkimlab/DiseaseInteractiveNetwork. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Yonghyun Nam, Sang-Hyuk Jung, Jae-Seung Yun, Vivek Sriram, Pankhuri Singhal, Marta Byrska-Bishop, Anurag Verma, Hyunjung Shin, Woong-Yang Park, Hong-Hee Won, Do Kyoon Kim
Bioinform.6
2018 Novel features and enhancements in BioBin, a tool for the biologically inspired binning and association analysis of rare variants
abstract
Motivation: BioBin is an automated bioinformatics tool for the multi-level biological binning of sequence variants. Herein, we present a significant update to BioBin which expands the software to facilitate a comprehensive rare variant analysis and incorporates novel features and analysis enhancements. Results: In BioBin 2.3, we extend our software tool by implementing statistical association testing, updating the binning algorithm, as well as incorporating novel analysis features providing for a robust, highly customizable, and unified rare variant analysis tool. Availability and implementation: The BioBin software package is open source and freely available to users at http://www.ritchielab.com/software/biobin-download. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Anna Okula Basile, Marta Byrska-Bishop, John R. Wallace, Alex Thomas Frase, Marylyn D. Ritchie
Bioinform.2