223 related articles for article (PubMed ID: 29390075)
1. IW-Scoring: an Integrative Weighted Scoring framework for annotating and prioritizing genetic variations in the noncoding genome.
Wang J; Dayem Ullah AZ; Chelala C
Nucleic Acids Res; 2018 May; 46(8):e47. PubMed ID: 29390075
[TBL] [Abstract][Full Text] [Related]
2. Res2s2aM: Deep residual network-based model for identifying functional noncoding SNPs in trait-associated regions.
Liu Z; Yao Y; Wei Q; Weeder B; Ramsey SA
Pac Symp Biocomput; 2019; 24():76-87. PubMed ID: 30864312
[TBL] [Abstract][Full Text] [Related]
3. LARVA: an integrative framework for large-scale analysis of recurrent variants in noncoding annotations.
Lochovsky L; Zhang J; Fu Y; Khurana E; Gerstein M
Nucleic Acids Res; 2015 Sep; 43(17):8123-34. PubMed ID: 26304545
[TBL] [Abstract][Full Text] [Related]
4. Altered TERT promoter and other genomic regulatory elements: occurrence and impact.
Heidenreich B; Kumar R
Int J Cancer; 2017 Sep; 141(5):867-876. PubMed ID: 28407294
[TBL] [Abstract][Full Text] [Related]
5. GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding.
Zeng H; Hashimoto T; Kang DD; Gifford DK
Bioinformatics; 2016 Feb; 32(4):490-6. PubMed ID: 26476779
[TBL] [Abstract][Full Text] [Related]
6. 3DSNP: a database for linking human noncoding SNPs to their three-dimensional interacting genes.
Lu Y; Quan C; Chen H; Bo X; Zhang C
Nucleic Acids Res; 2017 Jan; 45(D1):D643-D649. PubMed ID: 27789693
[TBL] [Abstract][Full Text] [Related]
7. OncoBase: a platform for decoding regulatory somatic mutations in human cancers.
Li X; Shi L; Wang Y; Zhong J; Zhao X; Teng H; Shi X; Yang H; Ruan S; Li M; Sun ZS; Zhan Q; Mao F
Nucleic Acids Res; 2019 Jan; 47(D1):D1044-D1055. PubMed ID: 30445567
[TBL] [Abstract][Full Text] [Related]
8. Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C.
Cornish AJ; Hoang PH; Dobbins SE; Law PJ; Chubb D; Orlando G; Houlston RS
Blood Adv; 2019 Jan; 3(1):21-32. PubMed ID: 30606723
[TBL] [Abstract][Full Text] [Related]
9. Convergent downstream candidate mechanisms of independent intergenic polymorphisms between co-classified diseases implicate epistasis among noncoding elements.
Han J; Li J; Achour I; Pesce L; Foster I; Li H; Lussier YA
Pac Symp Biocomput; 2018; 23():524-535. PubMed ID: 29218911
[TBL] [Abstract][Full Text] [Related]
10. Mapping and Making Sense of Noncoding Mutations in the Genome.
Yang J; Adli M
Cancer Res; 2019 Sep; 79(17):4309-4314. PubMed ID: 31387922
[TBL] [Abstract][Full Text] [Related]
11. Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer.
Fujimoto A; Furuta M; Totoki Y; Tsunoda T; Kato M; Shiraishi Y; Tanaka H; Taniguchi H; Kawakami Y; Ueno M; Gotoh K; Ariizumi S; Wardell CP; Hayami S; Nakamura T; Aikata H; Arihiro K; Boroevich KA; Abe T; Nakano K; Maejima K; Sasaki-Oku A; Ohsawa A; Shibuya T; Nakamura H; Hama N; Hosoda F; Arai Y; Ohashi S; Urushidate T; Nagae G; Yamamoto S; Ueda H; Tatsuno K; Ojima H; Hiraoka N; Okusaka T; Kubo M; Marubashi S; Yamada T; Hirano S; Yamamoto M; Ohdan H; Shimada K; Ishikawa O; Yamaue H; Chayama K; Miyano S; Aburatani H; Shibata T; Nakagawa H
Nat Genet; 2016 May; 48(5):500-9. PubMed ID: 27064257
[TBL] [Abstract][Full Text] [Related]
12. Genetic Predisposition to the Mortality in Septic Shock Patients: From GWAS to the Identification of a Regulatory Variant Modulating the Activity of a
Rosier F; Brisebarre A; Dupuis C; Baaklini S; Puthier D; Brun C; Pradel LC; Rihet P; Payen D
Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34072601
[TBL] [Abstract][Full Text] [Related]
13. Quantitative Trait Loci Identify Functional Noncoding Variation in Cancer.
Heyn H
PLoS Genet; 2016 Mar; 12(3):e1005826. PubMed ID: 26938653
[TBL] [Abstract][Full Text] [Related]
14. The humankind genome: from genetic diversity to the origin of human diseases.
Belizário JE
Genome; 2013 Dec; 56(12):705-16. PubMed ID: 24433206
[TBL] [Abstract][Full Text] [Related]
15. ReFeaFi: Genome-wide prediction of regulatory elements driving transcription initiation.
Umarov R; Li Y; Arakawa T; Takizawa S; Gao X; Arner E
PLoS Comput Biol; 2021 Sep; 17(9):e1009376. PubMed ID: 34491989
[TBL] [Abstract][Full Text] [Related]
16. Deep sequencing of 10,000 human genomes.
Telenti A; Pierce LC; Biggs WH; di Iulio J; Wong EH; Fabani MM; Kirkness EF; Moustafa A; Shah N; Xie C; Brewerton SC; Bulsara N; Garner C; Metzker G; Sandoval E; Perkins BA; Och FJ; Turpaz Y; Venter JC
Proc Natl Acad Sci U S A; 2016 Oct; 113(42):11901-11906. PubMed ID: 27702888
[TBL] [Abstract][Full Text] [Related]
17. An integrative scoring system for ranking SNPs by their potential deleterious effects.
Lee PH; Shatkay H
Bioinformatics; 2009 Apr; 25(8):1048-55. PubMed ID: 19228803
[TBL] [Abstract][Full Text] [Related]
18. An integrative and applicable phylogenetic footprinting framework for cis-regulatory motifs identification in prokaryotic genomes.
Liu B; Zhang H; Zhou C; Li G; Fennell A; Wang G; Kang Y; Liu Q; Ma Q
BMC Genomics; 2016 Aug; 17():578. PubMed ID: 27507169
[TBL] [Abstract][Full Text] [Related]
19. A Dual Model for Prioritizing Cancer Mutations in the Non-coding Genome Based on Germline and Somatic Events.
Li J; Poursat MA; Drubay D; Motz A; Saci Z; Morillon A; Michiels S; Gautheret D
PLoS Comput Biol; 2015 Nov; 11(11):e1004583. PubMed ID: 26588488
[TBL] [Abstract][Full Text] [Related]
20. Cancer regulatory variation.
Hennessey RC; Brown KM
Curr Opin Genet Dev; 2021 Feb; 66():41-49. PubMed ID: 33422949
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]