日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

In vivo mapping of mutagenesis sensitivity of human enhancers

人类增强子诱变敏感性的体内定位

Kosicki, Michael; Zhang, Boyang; Hecht, Vivian; Pampari, Anusri; Cook, Laura E; Slaven, Neil; Akiyama, Jennifer A; Plajzer-Frick, Ingrid; Novak, Catherine S; Kato, Momoe; Tran, Stella; Hunter, Riana D; von Maydell, Kianna; Barton, Sarah; Beckman, Erik; Zhu, Yiwen; Dickel, Diane E; Kundaje, Anshul; Visel, Axel; Pennacchio, Len A

Massively parallel reporter assays and mouse transgenic assays provide correlated and complementary information about neuronal enhancer activity.

大规模平行报告基因检测和转基因小鼠检测提供了关于神经元增强子活性的相关和互补信息

Kosicki Michael, Laboy Cintrón Dianne, Keukeleire Pia, Schubach Max, Page Nicholas F, Georgakopoulos-Soares Ilias, Akiyama Jennifer A, Plajzer-Frick Ingrid, Novak Catherine S, Kato Momoe, Hunter Riana D, von Maydell Kianna, Barton Sarah, Godfrey Patrick, Beckman Erik, Sanders Stephan J, Kircher Martin, Pennacchio Len A, Ahituv Nadav

VISTA Enhancer browser: an updated database of tissue-specific developmental enhancers

VISTA增强子浏览器:组织特异性发育增强子的最新数据库

Kosicki, Michael; Baltoumas, Fotis A; Kelman, Guy; Boverhof, Joshua; Ong, Yeongshnn; Cook, Laura E; Dickel, Diane E; Pavlopoulos, Georgios A; Pennacchio, Len A; Visel, Axel

ChromBPNet: bias factorized, base-resolution deep learning models of chromatin accessibility reveal cis-regulatory sequence syntax, transcription factor footprints and regulatory variants

ChromBPNet:基于偏差分解的、碱基分辨率的染色质可及性深度学习模型揭示顺式调控序列语法、转录因子足迹和调控变异

Pampari, Anusri; Shcherbina, Anna; Kvon, Evgeny Z; Kosicki, Michael; Nair, Surag; Kundu, Soumya; Kathiria, Arwa S; Risca, Viviana I; Kuningas, Kristiina; Alasoo, Kaur; Greenleaf, William James; Pennacchio, Len A; Kundaje, Anshul

Large-scale discovery of neural enhancers for cis-regulation therapies

大规模发现用于顺式调控疗法的神经增强剂

McDiarmid, Troy A; Page, Nicholas F; Chardon, Florence M; Daza, Riza M; Chen, George T; Kosicki, Michael; James, Lucas M; Nourie, Hannah C; Laboy-Cintrón, Dianne; Lee, Arthur S; Vij, Paula; Calderon, Diego; Lalanne, Jean-Benoît; Martin, Beth K; Fink, Kyle; Talkowski, Michael E; Muotri, Alysson R; Philpot, Benjamin D; Pennacchio, Len A; Geschwind, Daniel H; Sanders, Stephan J; Ahituv, Nadav; Shendure, Jay

A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders

一种基于细胞类型的框架,用于识别孟德尔遗传调控障碍中的非编码变异。

Lee, Arthur S; Ayers, Lauren J; Kosicki, Michael; Chan, Wai-Man; Fozo, Lydia N; Pratt, Brandon M; Collins, Thomas E; Zhao, Boxun; Rose, Matthew F; Sanchis-Juan, Alba; Fu, Jack M; Wong, Isaac; Zhao, Xuefang; Tenney, Alan P; Lee, Cassia; Laricchia, Kristen M; Barry, Brenda J; Bradford, Victoria R; Jurgens, Julie A; England, Eleina M; Lek, Monkol; MacArthur, Daniel G; Lee, Eunjung Alice; Talkowski, Michael E; Brand, Harrison; Pennacchio, Len A; Engle, Elizabeth C

Mutagenesis Sensitivity Mapping of Human Enhancers In Vivo

人类增强子体内诱变敏感性作图

Kosicki, Michael; Zhang, Boyang; Pampari, Anusri; Akiyama, Jennifer A; Plajzer-Frick, Ingrid; Novak, Catherine S; Tran, Stella; Zhu, Yiwen; Kato, Momoe; Hunter, Riana D; von Maydell, Kianna; Barton, Sarah; Beckman, Erik; Kundaje, Anshul; Dickel, Diane E; Visel, Axel; Pennacchio, Len A

Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart.

利用人类胎儿心脏调控图谱,研究先天性心脏缺陷风险变异的分子趋同性

Ma X Rosa, Conley Stephanie D, Kosicki Michael, Bredikhin Danila, Cui Ran, Tran Steven, Sheth Maya U, Qiu Wei-Lin, Chen Sijie, Kundu Soumya, Kang Helen Y, Amgalan Dulguun, Munger Chad J, Duan Lauren, Dang Katherine, Rubio Oriane Matthys, Kany Shinwan, Zamirpour Siavash, DePaolo John, Padmanabhan Arun, Olgin Jeffrey, Damrauer Scott, Andersson Robin, Gu Mingxia, Priest James R, Quertermous Thomas, Qiu Xiaojie, Rabinovitch Marlene, Visel Axel, Pennacchio Len, Kundaje Anshul, Glass Ian A, Gifford Casey A, Pirruccello James P, Goodyer William R, Engreitz Jesse M