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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2020 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 3 |
2024 | 1 |
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Page 1
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods.
Genome Biol. 2024 Feb 22;25(1):53. doi: 10.1186/s13059-023-03113-6.
Genome Biol. 2024.
PMID: 38389099
Free PMC article.
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants.
McAfee JC, Lee S, Lee J, Bell JL, Krupa O, Davis J, Insigne K, Bond ML, Zhao N, Boyle AP, Phanstiel DH, Love MI, Stein JL, Ruzicka WB, Davila-Velderrain J, Kosuri S, Won H.
McAfee JC, et al.
Cell Genom. 2023 Sep 15;3(10):100404. doi: 10.1016/j.xgen.2023.100404. eCollection 2023 Oct 11.
Cell Genom. 2023.
PMID: 37868037
Free PMC article.
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Challenges in screening for de novo noncoding variants contributing to genetically complex phenotypes.
Castro CP, Diehl AG, Boyle AP.
Castro CP, et al.
HGG Adv. 2023 May 20;4(3):100210. doi: 10.1016/j.xhgg.2023.100210. eCollection 2023 Jul 13.
HGG Adv. 2023.
PMID: 37305558
Free PMC article.
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Annotating and prioritizing human non-coding variants with RegulomeDB v.2.
Dong S, Zhao N, Spragins E, Kagda MS, Li M, Assis P, Jolanki O, Luo Y, Cherry JM, Boyle AP, Hitz BC.
Dong S, et al.
Nat Genet. 2023 May;55(5):724-726. doi: 10.1038/s41588-023-01365-3.
Nat Genet. 2023.
PMID: 37173523
Free PMC article.
No abstract available.
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Prioritization of regulatory variants with tissue-specific function in the non-coding regions of human genome.
Dong S, Boyle AP.
Dong S, et al.
Nucleic Acids Res. 2022 Jan 11;50(1):e6. doi: 10.1093/nar/gkab924.
Nucleic Acids Res. 2022.
PMID: 34648033
Free PMC article.
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F-Seq2: improving the feature density based peak caller with dynamic statistics.
Zhao N, Boyle AP.
Zhao N, et al.
NAR Genom Bioinform. 2021 Feb 23;3(1):lqab012. doi: 10.1093/nargab/lqab012. eCollection 2021 Mar.
NAR Genom Bioinform. 2021.
PMID: 33655209
Free PMC article.
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TRACE: transcription factor footprinting using chromatin accessibility data and DNA sequence.
Ouyang N, Boyle AP.
Ouyang N, et al.
Genome Res. 2020 Jul;30(7):1040-1046. doi: 10.1101/gr.258228.119. Epub 2020 Jul 6.
Genome Res. 2020.
PMID: 32660981
Free PMC article.
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