Summary of connectivity and size by depth (related to Fig. 5, Supplementary Fig. 1)

AN Aljoscha Nern
FL Frank Lösche
ST Shin-ya Takemura
LB Laura E Burnett
MD Marisa Dreher
EG Eyal Gruntman
JH Judith Hoeller
GH Gary B Huang
MJ Michał Januszewski
NK Nathan C Klapoetke
SK Sanna Koskela
KL Kit D Longden
ZL Zhiyuan Lu
SP Stephan Preibisch
WQ Wei Qiu
ER Edward M Rogers
PS Pavithraa Seenivasan
AZ Arthur Zhao
JB John Bogovic
BC Brandon S Canino
JC Jody Clements
MC Michael Cook
SF Samantha Finley-May
MF Miriam A Flynn
IH Imran Hameed
KH Kenneth J Hayworth
GH Gary Patrick Hopkins
PH Philip M Hubbard
WK William T Katz
JK Julie Kovalyak
SL Shirley A Lauchie
ML Meghan Leonard
AL Alanna Lohff
CM Charli A Maldonado
CM Caroline Mooney
NO Nneoma Okeoma
DO Donald J Olbris
CO Christopher Ordish
TP Tyler Paterson
EP Emily M Phillips
TP Tobias Pietzsch
JS Jennifer Rivas Salinas
PR Patricia K Rivlin
AS Ashley L Scott
LS Louis A Scuderi
ST Satoko Takemura
IT Iris Talebi
AT Alexander Thomson
ET Eric T Trautman
LU Lowell Umayam
ask Ask a question
Favorite

To produce the synapse distribution by depth, featured prominently in the Cell Type Catalog (Supplementary Fig. 1), we first identify all synapses of each target cell from the designated cell type. Using a k-dimensional tree, we find the nearest neighboring column pin by Euclidean distance for each presynapse and postsynapse. The depth property of the column pin associates each synapse with one of the 121 medulla, 76 lobula, or 51 lobula plate depth bins (see Defining column centerlines and ROIs). Across all neurons of a cell type, we calculate the mean count separately for presynapses and postsynapses, per depth. We smooth the distribution per brain region with a Savitzky-Golay filter (window size 5, 1st-order polynomials) before plotting on the left-side panel of the summary data figures. Separately we provide the percentage of synapses located within the AME over the cell type’s total number of synapses, again separated by presynapses and postsynapses.

To quantify each cell type’s size as a function of depth, we find the depth for all synapses. Since columns are implemented as ROIs in neuPrint (see Connectome data access overview), each synapse comes with an associated column. For each cell type, we calculate the mean count of columns with synapses (combining pre and post) per depth and smooth the distribution per brain region with a Savitzky-Golay filter (window size 5, 1st-order polynomials) before plotting on the right-most panel of the summary data.

The center panel of the cell type summary contains a connectivity summary. For all neurons of a target cell instance (effectively type, but separately accounting for right and left instances), we find all synapses and their connecting partner cells. We order them by the fraction of input and output connections and show the top five after removing unnamed segments.

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A