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

Evolutionary transfer learning enables organism-wide inference of mammalian enhancer landscapes

进化迁移学习能够对哺乳动物增强子图谱进行全生物体范围的推断

Qiu, Chengxiang; Daza, Riza M; Welsh, Ian C; Patwardhan, Rupali P; Martin, Beth K; Li, Tony; Yang, Shizhao; Kempynck, Niklas; Taylor, Megan L; Fulton, Olivia; Le, Truc-Mai; O'Day, Diana R; Lalanne, Jean-Benoît; Domcke, Silvia; Murray, Stephen A; Aerts, Stein; Trapnell, Cole; Shendure, Jay

Massively parallel characterization of transcriptional regulatory elements

转录调控元件的大规模并行表征

Agarwal, Vikram; Inoue, Fumitaka; Schubach, Max; Penzar, Dmitry; Martin, Beth K; Dash, Pyaree Mohan; Keukeleire, Pia; Zhang, Zicong; Sohota, Ajuni; Zhao, Jingjing; Georgakopoulos-Soares, Ilias; Noble, William S; Yardımcı, Galip Gürkan; Kulakovskiy, Ivan V; Kircher, Martin; Shendure, Jay; Ahituv, Nadav

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

Lineage recording in monoclonal gastruloids reveals heritable modes of early development.

单克隆原肠胚谱系记录揭示了早期发育的可遗传模式

Regalado Samuel G, Qiu Chengxiang, Kottapalli Sanjay, Martin Beth K, Chen Wei, Liao Hanna, Kim Haedong, Li Xiaoyi, Lalanne Jean-Benoît, Hamazaki Nobuhiko, Domcke Silvia, Choi Junhong, Shendure Jay

Chromatin context-dependent regulation and epigenetic manipulation of prime editing.

染色质环境依赖性调控和表观遗传操纵主要编辑

Li Xiaoyi, Chen Wei, Martin Beth K, Calderon Diego, Lee Choli, Choi Junhong, Chardon Florence M, McDiarmid Troy A, Daza Riza M, Kim Haedong, Lalanne Jean-Benoît, Nathans Jenny F, Lee David S, Shendure Jay

Single-cell analysis of chromatin and expression reveals age- and sex-associated alterations in the human heart

单细胞染色质和表达分析揭示了人类心脏中与年龄和性别相关的改变

Read, David F; Booth, Gregory T; Daza, Riza M; Jackson, Dana L; Gladden, Rula Green; Srivatsan, Sanjay R; Ewing, Brent; Franks, Jennifer M; Spurrell, Cailyn H; Gomes, Anne Roshella; O'Day, Diana; Gogate, Aishwarya A; Martin, Beth K; Larson, Haleigh; Pfleger, Christian; Starita, Lea; Lin, Yiing; Shendure, Jay; Lin, Shin; Trapnell, Cole

Chromatin context-dependent regulation and epigenetic manipulation of prime editing

染色质环境依赖性调控和表观遗传操纵对主要编辑的影响

Li, Xiaoyi; Chen, Wei; Martin, Beth K; Calderon, Diego; Lee, Choli; Choi, Junhong; Chardon, Florence M; McDiarmid, Troy; Kim, Haedong; Lalanne, Jean-Benoît; Nathans, Jenny F; Shendure, Jay

Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative

针对参与“我的生命,我们的未来”计划的3000名血友病患者,我们提出了一种新的基因分析方法并取得了成果。

Johnsen, Jill M; Fletcher, Shelley N; Huston, Haley; Roberge, Sarah; Martin, Beth K; Kircher, Martin; Josephson, Neil C; Shendure, Jay; Ruuska, Sarah; Koerper, Marion A; Morales, Jaime; Pierce, Glenn F; Aschman, Diane J; Konkle, Barbara A

The haplotype-resolved genome and epigenome of the aneuploid HeLa cancer cell line

非整倍体HeLa癌细胞系的单倍型解析基因组和表观基因组

Adey, Andrew; Burton, Joshua N; Kitzman, Jacob O; Hiatt, Joseph B; Lewis, Alexandra P; Martin, Beth K; Qiu, Ruolan; Lee, Choli; Shendure, Jay

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

多重靶向测序可识别自闭症谱系障碍中的复发性突变基因

O'Roak, Brian J; Vives, Laura; Fu, Wenqing; Egertson, Jarrett D; Stanaway, Ian B; Phelps, Ian G; Carvill, Gemma; Kumar, Akash; Lee, Choli; Ankenman, Katy; Munson, Jeff; Hiatt, Joseph B; Turner, Emily H; Levy, Roie; O'Day, Diana R; Krumm, Niklas; Coe, Bradley P; Martin, Beth K; Borenstein, Elhanan; Nickerson, Deborah A; Mefford, Heather C; Doherty, Dan; Akey, Joshua M; Bernier, Raphael; Eichler, Evan E; Shendure, Jay