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Logan Spector

dblp:367/1663 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2024
0000-0003-2516-0222ORCID · reported

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 › genomics › genome-wide association study
multi-trait association testing
0.812024
Subset scanning for multi-trait analysis using GWAS summary statistics · Bioinform. 2024
Bioinformatics and computational biology › statistical genetics › genotype-phenotype analysis
pleiotropy analysis
0.812024
Subset scanning for multi-trait analysis using GWAS summary statistics · Bioinform. 2024
Bioinformatics and computational biology
statistical genetics
0.812024
Subset scanning for multi-trait analysis using GWAS summary statistics · Bioinform. 2024

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

subset scanning · 0.8GWAS summary statistics · 0.8
YearPublicationVenuePosition
2024 Subset scanning for multi-trait analysis using GWAS summary statistics
abstract
MOTIVATION: Multi-trait analysis has been shown to have greater statistical power than single-trait analysis. Most of the existing multi-trait analysis methods only work with a limited number of traits and usually prioritize high statistical power over identifying relevant traits, which heavily rely on domain knowledge. RESULTS: To handle diseases and traits with obscure etiology, we developed TraitScan, a powerful and fast algorithm that identifies potential pleiotropic traits from a moderate or large number of traits (e.g. dozens to thousands) and tests the association between one genetic variant and the selected traits. TraitScan can handle either individual-level or summary-level GWAS data. We evaluated TraitScan using extensive simulations and found that it outperformed existing methods in terms of both testing power and trait selection when sparsity was low or modest. We then applied it to search for traits associated with Ewing Sarcoma, a rare bone tumor with peak onset in adolescence, among 754 traits in UK Biobank. Our analysis revealed a few promising traits worthy of further investigation, highlighting the use of TraitScan for more effective multi-trait analysis as biobanks emerge. We also extended TraitScan to search and test association with a polygenic risk score and genetically imputed gene expression. AVAILABILITY AND IMPLEMENTATION: Our algorithm is implemented in an R package "TraitScan" available at https://github.com/RuiCao34/TraitScan.
Evan Olawsky, Edward McFowland, Erin Marcotte, Logan Spector, Tianzhong Yang
Bioinform.5