Functional connectomics spanning multiple areas of mouse visual cortex

Author:

,Bae J. AlexanderORCID,Baptiste Mahaly,Bodor Agnes L.,Brittain Derrick,Buchanan JoAnnORCID,Bumbarger Daniel J.,Castro Manuel A.,Celii Brendan,Cobos Erick,Collman Forrest,da Costa Nuno MaçaricoORCID,Dorkenwald SvenORCID,Elabbady Leila,Fahey Paul G.ORCID,Fliss Tim,Froudarakis Emmanouil,Gager Jay,Gamlin Clare,Halageri Akhilesh,Hebditch James,Jia Zhen,Jordan Chris,Kapner Daniel,Kemnitz NicoORCID,Kinn Sam,Koolman Selden,Kuehner Kai,Lee Kisuk,Li Kai,Lu Ran,Macrina ThomasORCID,Mahalingam Gayathri,McReynolds Sarah,Miranda Elanine,Mitchell Eric,Mondal Shanka Subhra,Moore Merlin,Mu Shang,Muhammad Taliah,Nehoran Barak,Ogedengbe Oluwaseun,Papadopoulos Christos,Papadopoulos SteliosORCID,Patel Saumil,Pitkow XaqORCID,Popovych Sergiy,Ramos Anthony,Reid R. Clay,Reimer Jacob,Schneider-Mizell Casey M.ORCID,Seung H. SebastianORCID,Silverman Ben,Silversmith WilliamORCID,Sterling Amy,Sinz Fabian H.,Smith Cameron L.ORCID,Suckow Shelby,Takeno MarcORCID,Tan Zheng H.,Tolias Andreas S.,Torres Russel,Turner Nicholas L.ORCID,Walker Edgar Y.ORCID,Wang TianyuORCID,Williams GraceORCID,Williams Sarah,Willie Kyle,Willie Ryan,Wong William,Wu JingpengORCID,Xu Chris,Yang RunzheORCID,Yatsenko Dimitri,Ye Fei,Yin Wenjing,Yu Szi-chieh

Abstract

ABSTRACTThe value of an integrated approach for understanding the neocortex by combining functional characterization of single neuron activity with the underlying circuit architecture has been understood since the dawn of modern neuroscience. However, in practice, anatomical connectivity and physiology have been studied mostly separately. Following in the footsteps of previous studies that have combined physiology and anatomy in the same tissue, here we present a unique functional connectomics dataset that contains calcium imaging of an estimated 75,000 neurons from primary visual cortex (VISp) and three higher visual areas (VISrl, VISal and VISlm), that were recorded while a mouse viewed natural movies and parametric stimuli. The functional data were co-registered with electron microscopy (EM) data of the same volume which were automatically segmented, reconstructing more than 200,000 cells (neuronal and non-neuronal) and 524 million synapses. Subsequent proofreading of some neurons in this volume yielded reconstructions that include complete dendritic trees as well the local and inter-areal axonal projections. The largest proofread excitatory axon reached a length of 19 mm and formed 1893 synapses, while the largest inhibitory axon formed 10081 synapses. Here we release this dataset as an open access resource to the scientific community including a set of analysis tools that allows easy data access, both programmatically and through a web user interface.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3