Xizhe Zhang

Network topology
is reflected
within neurons.

FlyScope · Connectome Explorer

Inside a neuron, where inputs land reflects connections elsewhere in the network.

01 / Connectome explorer Scroll to explore

02 / The question

Look inside
the node.

A connectivity graph draws each neuron as a point. Inside, every input lands somewhere on the cell’s branches. Does that internal arrangement record connections elsewhere in the network?

  1. 01

    Fix a connection. Partner B contacts receiving neuron C: five or more records one way, fewer than five back.

  2. 02

    Map the inputs. Each source input on C is measured along C’s own branches to the nearest input from B in the same brain region.

  3. 03

    Read the far edge. Sources wired to B, an edge that never touches C, land nearer B’s inputs. Input maps alone then predict A→B for unseen sources.

? A B C Source A Partner B Receiver C Inside C
The edge A→B never touches C, yet it shows in where A and B land on C. Inputs from AInputs from BOther inputs

Held fixed receiver and brain region · paths along C’s own branches · source cells withheld from fitting

Schematic
FlyScope03 / Shared input

One receiver. Multiple inputs.

Shared input

Inspect where sources meet.

Compare input locations on a shared receiving neuron. Inputs from a source shared with partner B lie nearer B’s inputs.

  • Receiver C
  • Source A
  • Partner B

Each point is an input on receiver C, coloured by its source.

Open shared input
Schematic · not to scale

04 / Paper findings

Follow the finding.

From network connections to input locations.

  1. 01Network topology
  2. 02Receiving neuron
  3. 03Input organization
Open paper example
Input locations

Source APartner B

Move from a circuit to its receiving neuron.

Schematic

05 / Results

Two fly brains. One direction.

The same relationship in MaleCNS and FlyWire, under three increasingly strict tests.

01 / Between sources

Shared sources sit closer

Mean path from a source input on C to the nearest partner input: sources that also contact B against all other sources.

−9.42 µm
MaleCNS · 95% −10.52 to −8.31
−7.98 µm
FlyWire · 95% −9.27 to −6.70

Negative in 82.7% of 1,079 MaleCNS and 80.7% of 720 FlyWire receivers; 13,318 and 5,807 connections.

02 / Fixed inputs

Same inputs, different partners

Source A, receiver C and A’s inputs held fixed; partners that receive A input against partners with none, at three reference sites each.

−9.14 µm
MaleCNS · 95% −11.21 to −7.07
−10.15 µm
FlyWire · 95% −12.15 to −8.14

Same ordering in 749 of 922 MaleCNS and 483 of 589 FlyWire receivers.

03 / Unseen sources

Input maps predict connections

Predicting A→B for 200 test sources disjoint from 200 training sources, from input maps on known receivers.

0.161 AP
MaleCNS · from 0.089 with counts and size only
0.114 AP
FlyWire · from 0.069

Log loss 0.184 → 0.165 and 0.142 → 0.125; 30,702 and 21,822 scored pairs. Point estimates from one source split per specimen.

Beyond the fly brains, two adult C. elegans reconstructions also gave negative within-source differences (10 and 13 receivers), and a Platynereis larval population was too sparse to decide. These are associations within single specimens: anatomical opportunity, selective wiring, or both remain compatible.

Explore the connectome.

Find a neuron. Follow its connections.

PNGCSV

Interface preview · schematic arbor

08 / The paper

Read the study.

Xizhe Zhang · Manuscript, 2026

Synaptic organization in shared receivers predicts connectivity between input neurons

Abstract

A neuronal connectivity graph records which cells are connected but discards the positions at which their inputs enter a receiving neuron. We asked whether this internal arrangement contains information about connections between the input neurons themselves. In two adult Drosophila connectomes, inputs from sources connected to a descending-neuron partner lay nearer that partner’s inputs on a shared receiver. Mean path-distance differences were 9.4 µm in MaleCNS and 8.0 µm in FlyWire. With source-input positions fixed and reference-site counts standardized, the relationship persisted across alternative partners. We then used source-labelled input maps on known receivers to predict connections between source cells excluded from model fitting. Adding spatial-distribution and distance features to input counts and receiver size increased average precision from 0.089 to 0.161 in MaleCNS and from 0.069 to 0.114 in FlyWire, with lower probability loss in both datasets. Predictions averaged information across eligible shared receivers. These findings connect the organization of inputs within neurons to connectivity among their sources and show that this spatial information is useful for inferring connections between unseen input cells.

  • synaptic organization
  • connectomics
  • physical networks
  • descending neurons
  • Drosophila

Data & sources

Public reconstructions, unchanged.

FlyScope reads released connectome data without altering it. No new animals were acquired. Each dataset represents one animal.

MaleCNS v1.0
One male central nervous system: contact records (confidence ≥ 0.5), annotations and skeletons.
male-cns.janelia.org ↗
FlyWire / FAFB v783
One female brain: synapses, connectivity, matching skeletons and annotations.
zenodo 10676866 ↗ · zenodo 10877326 ↗
BANC v888
Brain-and-cord network background and identified cord-output analyses.
doi:10.7910/DVN/7WTH1N ↗
C. elegans · Dataset 7 & 8
Two adult reconstructions used for exploratory placement comparisons.
dwitvliet/nature2021 ↗
Platynereis
Three-day larval head-to-trunk projection cohort; sparse and exploratory.
JekelyLab ↗

The neuron drawings on this page are schematic illustrations. The explorer shows recorded skeletons and synapse coordinates.

Paper · Zhang X. Synaptic organization in shared receivers predicts connectivity between input neurons.

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