In one paragraphArticle in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from itWhat it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registryThe trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
3 · Its place in the literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
8 authors.
Yueyang HuangBioinformatics Research Center, North Carolina State University, 1 Lampe Drive, Raleigh, NC 27607, United States.ORCID 0009-0007-1441-2881 Riddhik BasuDepartment of Statistics, North Carolina State University, 2311 Stinson Drive, Raleigh, NC 27607, United States.ORCID 0009-0007-6433-3321 Yuhuan ChengBioinformatics Research Center, North Carolina State University, 1 Lampe Drive, Raleigh, NC 27607, United States.ORCID 0009-0003-1465-075X Wenbin LuDepartment of Statistics, North Carolina State University, 2311 Stinson Drive, Raleigh, NC 27607, United States.ORCID 0000-0002-7320-4755 Shannon T HollowayDepartment of Population Health Sciences, Duke University, 215 Morris Street, Durham, NC 27701, United States.ORCID 0009-0005-6757-7503 Chang ChenDepartment of Biostatistics, University of North Carolina at Chapel Hill, 135 Dauer Drive, Chapel Hill, NC 27599, United States.ORCID 0009-0001-4136-0876 Yun LiDepartment of Biostatistics, University of North Carolina at Chapel Hill, 135 Dauer Drive, Chapel Hill, NC 27599, United States.ORCID 0000-0002-9275-4189 Jung-Ying TzengBioinformatics Research Center, North Carolina State University, 1 Lampe Drive, Raleigh, NC 27607, United States.ORCID 0000-0002-5505-1775 Funding
The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3MStudies of Rare Genetic Variation in the Isolated Population of SardiniaR01HL117626 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2013 to 2016
$10.5MRare variants and NHLBI traits in deeply phenotyped cohortsR01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2014 to 2016
$8.9MNext generation functional genomics of hematology traitsR01HL146500 · NHLBI · UNIVERSITY OF WASHINGTON · PI ALEXANDER P REINER · 2020 to 2026
$5.7MRare variants and NHLBI traits in deeply phenotyped cohortsU01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2017 to 2018
$5.6MDetermining the Genetic Basis of Hidradenitis SuppurativaR01AR083790 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yun Li, KAREN L. MOHLKE · 2024 to 2026
$1.3MNHGRI NIH HHS U54 HG003273NHLBI NIH HHS HHSN268201500015CNHLBI NIH HHS HHSN268201700001CNHLBI NIH HHS HHSN268201700001INHLBI NIH HHS HHSN268201700002CNHLBI NIH HHS HHSN268201700002INHLBI NIH HHS HHSN268201700003CNHLBI NIH HHS HHSN268201700003INHLBI NIH HHS HHSN268201700004CNHLBI NIH HHS HHSN268201700004INHLBI NIH HHS HHSN268201700005CNHLBI NIH HHS HHSN268201700005INHLBI NIH HHS HHSN268201800001CNHLBI NIH HHS R01 HL117626NHLBI NIH HHS R01 HL120393NHLBI NIH HHS R01 HL146500NHLBI NIH HHS U01 HL120393NIAMS NIH HHS R01 AR083790NIH HHS R01AR083790NIH HHS R01HL146500NIH HHS RF1/R01AG074328
6 · The paper itselfAbstract
Variant-set association analysis is a powerful strategy for genetic studies of whole-genome sequence (WGS) data, especially for rare variants. By aggregating variant signals, variant-set analysis can improve statistical power, result interpretability, and study replicability. Motivated by the evidence that 3D genome architecture plays a critical role in regulating gene transcription, several works have incorporated 3D genome architecture into gene-based association tests and demonstrated great promise. In this work, we extend the idea of 3D-genome guided test from gene-centric to gene-agnostic, whole-genome testing by introducing an Hi-C informed kernel association test (i.e. HiC-KAT). We present a principled procedure that converts Hi-C contact confidence into borrowing weights and integrates these weights into genetic similarity kernels so that higher-confidence interacting loci contribute more to the association test of the target variant set. We use a controlling parameter to adaptively determine the appropriate degree of information borrowing from its interacting loci during association testing. We assess the performance of HiC-KAT using simulations and illustrate its advantage in detecting rare-variant sets using WGS data from the ARIC study in the Trans-Omics for Precision Medicine program.
Indexed as
Genetic VariationGenome, HumanGenome-Wide Association StudyGenomicsAlgorithmsHumanschromatin interactionsHi-C dataHi-C guided association testHi-C informed SKATkernel machine regressionrare-variant test
Identifiers
PMID42480046
PMCPMC13387501
What OpenQuestion holds
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LicenceCC BY-NC
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