374 related articles for article (PubMed ID: 30478436)
1. High-resolution genetic mapping of putative causal interactions between regions of open chromatin.
Kumasaka N; Knights AJ; Gaffney DJ
Nat Genet; 2019 Jan; 51(1):128-137. PubMed ID: 30478436
[TBL] [Abstract][Full Text] [Related]
2. Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes.
Song M; Yang X; Ren X; Maliskova L; Li B; Jones IR; Wang C; Jacob F; Wu K; Traglia M; Tam TW; Jamieson K; Lu SY; Ming GL; Li Y; Yao J; Weiss LA; Dixon JR; Judge LM; Conklin BR; Song H; Gan L; Shen Y
Nat Genet; 2019 Aug; 51(8):1252-1262. PubMed ID: 31367015
[TBL] [Abstract][Full Text] [Related]
3. CRISPR-Cas9 epigenome editing enables high-throughput screening for functional regulatory elements in the human genome.
Klann TS; Black JB; Chellappan M; Safi A; Song L; Hilton IB; Crawford GE; Reddy TE; Gersbach CA
Nat Biotechnol; 2017 Jun; 35(6):561-568. PubMed ID: 28369033
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide analysis of chromatin accessibility using ATAC-seq.
Shashikant T; Ettensohn CA
Methods Cell Biol; 2019; 151():219-235. PubMed ID: 30948010
[TBL] [Abstract][Full Text] [Related]
5. Assessment of 3D Interactions Between Promoters and Distal Regulatory Elements with Promoter Capture Hi-C (PCHi-C).
Karasu N; Sexton T
Methods Mol Biol; 2021; 2351():229-248. PubMed ID: 34382193
[TBL] [Abstract][Full Text] [Related]
6. Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus.
Chang H; Cai X; Li HJ; Liu WP; Zhao LJ; Zhang CY; Wang JY; Liu JW; Ma XL; Wang L; Yao YG; Luo XJ; Li M; Xiao X
Biol Psychiatry; 2021 Feb; 89(3):246-255. PubMed ID: 33246552
[TBL] [Abstract][Full Text] [Related]
7. Coupled Single-Cell CRISPR Screening and Epigenomic Profiling Reveals Causal Gene Regulatory Networks.
Rubin AJ; Parker KR; Satpathy AT; Qi Y; Wu B; Ong AJ; Mumbach MR; Ji AL; Kim DS; Cho SW; Zarnegar BJ; Greenleaf WJ; Chang HY; Khavari PA
Cell; 2019 Jan; 176(1-2):361-376.e17. PubMed ID: 30580963
[TBL] [Abstract][Full Text] [Related]
8. Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C.
Dryden NH; Broome LR; Dudbridge F; Johnson N; Orr N; Schoenfelder S; Nagano T; Andrews S; Wingett S; Kozarewa I; Assiotis I; Fenwick K; Maguire SL; Campbell J; Natrajan R; Lambros M; Perrakis E; Ashworth A; Fraser P; Fletcher O
Genome Res; 2014 Nov; 24(11):1854-68. PubMed ID: 25122612
[TBL] [Abstract][Full Text] [Related]
9. Detection of Short-Range DNA Interactions in Mammalian Cells Using High-Resolution Circular Chromosome Conformation Capture Coupled to Deep Sequencing.
Millau JF; Gaudreau L
Methods Mol Biol; 2015; 1334():245-59. PubMed ID: 26404155
[TBL] [Abstract][Full Text] [Related]
10. Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
Li MJ; Yan B; Sham PC; Wang J
Brief Bioinform; 2015 May; 16(3):393-412. PubMed ID: 24916300
[TBL] [Abstract][Full Text] [Related]
11. Developments in high-throughput functional epigenomics: CRISPR-single-cell assay for transposase-accessible chromatin using sequencing screens.
E Yan R; P Greenfield J; Dahmane N
Epigenomics; 2022 Jun; 14(11):645-649. PubMed ID: 35574596
[TBL] [Abstract][Full Text] [Related]
12. Mapping the functional impact of non-coding regulatory elements in primary T cells through single-cell CRISPR screens.
Alda-Catalinas C; Ibarra-Soria X; Flouri C; Gordillo JE; Cousminer D; Hutchinson A; Sun B; Pembroke W; Ullrich S; Krejci A; Cortes A; Acevedo A; Malla S; Fishwick C; Drewes G; Rapiteanu R
Genome Biol; 2024 Feb; 25(1):42. PubMed ID: 38308274
[TBL] [Abstract][Full Text] [Related]
13. Assay for transposase-accessible chromatin and circularized chromosome conformation capture, two methods to explore the regulatory landscapes of genes in zebrafish.
Fernández-Miñán A; Bessa J; Tena JJ; Gómez-Skarmeta JL
Methods Cell Biol; 2016; 135():413-30. PubMed ID: 27443938
[TBL] [Abstract][Full Text] [Related]
14. Assessing Chromatin Accessibility During WBR in Acoels.
Gehrke AR; Srivastava M
Methods Mol Biol; 2022; 2450():549-561. PubMed ID: 35359328
[TBL] [Abstract][Full Text] [Related]
15. Functional Genetic Variants Revealed by Massively Parallel Precise Genome Editing.
Sharon E; Chen SA; Khosla NM; Smith JD; Pritchard JK; Fraser HB
Cell; 2018 Oct; 175(2):544-557.e16. PubMed ID: 30245013
[TBL] [Abstract][Full Text] [Related]
16. Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues.
Brown AA; Viñuela A; Delaneau O; Spector TD; Small KS; Dermitzakis ET
Nat Genet; 2017 Dec; 49(12):1747-1751. PubMed ID: 29058714
[TBL] [Abstract][Full Text] [Related]
17. Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq.
Grbesa I; Tannenbaum M; Sarusi-Portuguez A; Schwartz M; Hakim O
J Vis Exp; 2017 Nov; (129):. PubMed ID: 29155775
[TBL] [Abstract][Full Text] [Related]
18. ChIATAC is an efficient strategy for multi-omics mapping of 3D epigenomes from low-cell inputs.
Chai H; Tjong H; Li P; Liao W; Wang P; Wong CH; Ngan CY; Leonard WJ; Wei CL; Ruan Y
Nat Commun; 2023 Jan; 14(1):213. PubMed ID: 36639381
[TBL] [Abstract][Full Text] [Related]
19. Strategies to identify causal common genetic variants and corresponding effector genes for paediatric obesity.
Littleton SH; Grant SFA
Pediatr Obes; 2022 Dec; 17(12):e12968. PubMed ID: 35971868
[TBL] [Abstract][Full Text] [Related]
20. Dynamic regulatory elements in single-cell multimodal data implicate key immune cell states enriched for autoimmune disease heritability.
Gupta A; Weinand K; Nathan A; Sakaue S; Zhang MJ; ; Donlin L; Wei K; Price AL; Amariuta T; Raychaudhuri S
Nat Genet; 2023 Dec; 55(12):2200-2210. PubMed ID: 38036783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
