What is in pipeline run 20261010
p3 = pdb.p3.k8s (this run) vs pdb = the current release (http://pdb.pdb.svc:7474).
Counts from VFB_reporting's own report queries, as published nightly in
VFB_reporting_results. Generated 2026-10-11 05:21 UTC — once per pipeline run.
Owlery for this run: owl.p3.k8s.
Datasets (production)
193
+0 vs pdb (193)
Individuals in datasets
1,039,514
+83,097 vs pdb (956,417)
Nodes (sum over labels)
13,057,565
+58,670 vs pdb (12,998,895)
Relationships
44,975,636
-62,560,115 vs pdb (107,535,751)
Datasets
| Dataset | individuals | NBLAST | NBLASTexp | ontology_terms | exp_cur | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| pdb | p3 | Δ | pdb | p3 | Δ | pdb | p3 | Δ | pdb | p3 | Δ | pdb | p3 | Δ | |
| Andrade2019 EM L1 Andrade et al. 2019 | 847 | 847 | 0 | 847 | 0 | -847 (-100.0%) | 0 | 0 | 0 | 27 | 27 | 0 | 0 | 0 | 0 |
| Aso2014 MBONs and split-GAL4 lines that target them (Aso2014) | 3,195 | 4,606 | +1,411 (+44.2%) | 0 | 0 | 0 | 787 | 0 | -787 (-100.0%) | 109 | 112 | +3 (+2.8%) | 0 | 0 | 0 |
| AsoRubin2016 split-GAL4 lines for dopaminergic neurons (AsoRubin2016) | 31 | 49 | +18 (+58.1%) | 0 | 0 | 0 | 3 | 0 | -3 (-100.0%) | 12 | 12 | 0 | 0 | 0 | 0 |
| Baltruschat2021 EM FAFB Baltruschat et al 2021 | 20 | 20 | 0 | 1 | 0 | -1 (-100.0%) | 19 | 0 | -19 (-100.0%) | 8 | 8 | 0 | 0 | 0 | 0 |
| Barnes2022 EM L1 Barnes et al., 2022 | 51 | 51 | 0 | 51 | 0 | -51 (-100.0%) | 0 | 0 | 0 | 26 | 26 | 0 | 0 | 0 | 0 |
| Bates2025 Brain and Nerve Cord (BANC) version 626 connectome neurons from Bates et al. (2025). | 80,505 | 80,505 | 0 | 23,934 | 0 | -23,934 (-100.0%) | 0 | 0 | 0 | 9,617 | 9,617 | 0 | 0 | 0 | 0 |
| Bates2026 Brain and Nerve Cord (BANC) version 888 connectome neurons from Bates et al. (2026). | 145,948 | 145,948 | 0 | 21,082 | 0 | -21,082 (-100.0%) | 0 | 0 | 0 | 10,672 | 10,672 | 0 | 0 | 0 | 0 |
| Bates2026roi BANC neuropil, tract and nerve ROIs | 305 | 305 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 155 | 155 | 0 | 0 | 0 | 0 |
| BatesSchlegel2020 EM FAFB Bates and Schlegel et al 2020 | 583 | 583 | 0 | 159 | 0 | -159 (-100.0%) | 277 | 0 | -277 (-100.0%) | 200 | 200 | 0 | 0 | 0 | 0 |
| Berck2016 Larval olfactory system neurons - EM (Berk2016) | 161 | 161 | 0 | 161 | 0 | -161 (-100.0%) | 0 | 0 | 0 | 82 | 82 | 0 | 0 | 0 | 0 |
| Berg2025 Male CNS version 0.9 connectome neurons from Berg et al. (2025). | 166,681 | 166,681 | 0 | 164,459 | 0 | -164,459 (-100.0%) | 0 | 0 | 0 | 10,348 | 10,348 | 0 | 0 | 0 | 0 |
| Berg2025a Male CNS version 1.0 connectome neurons from Berg et al. (2025). | 166,693 | 166,693 | 0 | 164,457 | 0 | -164,457 (-100.0%) | 0 | 0 | 0 | 10,348 | 10,348 | 0 | 0 | 0 | 0 |
| Berg2025aroi Male CNS neuropil ROIs | 396 | 396 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 212 | 212 | 0 | 0 | 0 | 0 |
| BrainName_Ito_half_brain BrainName neuropils and tracts - Ito half-brain | 76 | 76 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 75 | 75 | 0 | 0 | 0 | 0 |
| Burgos2018 Nociceptive system neurons - EM (Burgos2017) | 95 | 95 | 0 | 95 | 0 | -95 (-100.0%) | 0 | 0 | 0 | 54 | 54 | 0 | 0 | 0 | 0 |
| Cachero2010 Adult Brain fru clones (Cachero2010) | 119 | 119 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 84 | 84 | 0 | 0 | 0 | 0 |
| CarreiraRosario2018 EM L1 Carreira-Rosario, Arzan Zarin, Clark et al. 2018 | 31 | 31 | 0 | 31 | 0 | -31 (-100.0%) | 0 | 0 | 0 | 17 | 17 | 0 | 0 | 0 | 0 |
| Chiang2010 FlyCircuit 1.0 - single neurons (Chiang2010) | 16,127 | 16,127 | 0 | 15,929 | 0 | -15,929 (-100.0%) | 5,952 | 0 | -5,952 (-100.0%) | 216 | 215 | -1 (-0.5%) | 0 | 0 | 0 |
| Coates2020 EM FAFB Coates et al 2020 | 191 | 191 | 0 | 55 | 0 | -55 (-100.0%) | 10 | 0 | -10 (-100.0%) | 22 | 22 | 0 | 0 | 0 | 0 |
| Court2017 Adult VNS neuropils (Court2017) | 23 | 23 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 23 | 23 | 0 | 0 | 0 | 0 |
| Court2020 Adult VNC neuropils (Court2020) | 21 | 21 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 20 | 20 | 0 | 0 | 0 | 0 |
| Dickson2017 Dickson lab VT lines - FlyLight/Janelia images (2017) | 5,378 | 5,378 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2,530 | 2,530 | 0 | 0 | 0 | 0 |
| Dickson_VT Dickson lab VT line collection - VDRC images | 18,016 | 18,016 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 7,807 | 7,806 | -1 (-0.0%) | 0 | 0 | 0 |
| Dolan2018 EM FAFB Dolan and Belliart-Guerin et al. 2018 | 10 | 10 | 0 | 5 | 0 | -5 (-100.0%) | 10 | 0 | -10 (-100.0%) | 4 | 4 | 0 | 0 | 0 | 0 |
| Dolan2019 GAL4 Split expression patterns from Dolan et al. 2019 | 358 | 4,371 | +4,013 (+1120.9%) | 0 | 0 | 0 | 42 | 0 | -42 (-100.0%) | 111 | 114 | +3 (+2.7%) | 0 | 0 | 0 |
| Dombrovski2023 EM FAFB Dombrovski et al 2023 | 59 | 59 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 5 | 5 | 0 | 0 | 0 | 0 |
| Dorkenwald2023 FlyWire connectome neurons | 139,255 | 139,255 | 0 | 139,242 | 0 | -139,242 (-100.0%) | 0 | 0 | 0 | 7,574 | 7,574 | 0 | 0 | 0 | 0 |
| Dorkenwald2023roi FlyWire FAFB neuropil ROIs | 78 | 78 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 43 | 43 | 0 | 0 | 0 | 0 |
| Eichler2017 Larval MB neurons - EM (Eichler2017) | 388 | 388 | 0 | 388 | 0 | -388 (-100.0%) | 0 | 0 | 0 | 79 | 79 | 0 | 0 | 0 | 0 |
| Engert2022 EM FAFB Engert et al. 2022 | 144 | 144 | 0 | 131 | 0 | -131 (-100.0%) | 0 | 0 | 0 | 5 | 5 | 0 | 0 | 0 | 0 |
| Erginkaya2025 EM FAFB Erginkaya et al 2025 | 91 | 91 | 0 | 0 | 0 | 0 | 2 | 0 | -2 (-100.0%) | 35 | 35 | 0 | 0 | 0 | 0 |
| Eschbach2020 EM L1 Eschbach et al 2020 | 204 | 204 | 0 | 204 | 0 | -204 (-100.0%) | 0 | 0 | 0 | 108 | 108 | 0 | 0 | 0 | 0 |
| Eschbach2020b EM L1 Eschbach et al 2020b | 654 | 654 | 0 | 654 | 0 | -654 (-100.0%) | 0 | 0 | 0 | 95 | 95 | 0 | 0 | 0 | 0 |
| FafbDolan2019 EM FAFB Dolan et al. 2019 | 113 | 113 | 0 | 69 | 0 | -69 (-100.0%) | 104 | 0 | -104 (-100.0%) | 86 | 86 | 0 | 0 | 0 | 0 |
| Felsenberg2018 EM FAFB Felsenberg et al. 2018 | 3 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | -3 (-100.0%) | 3 | 3 | 0 | 0 | 0 | 0 |
| FlyLight2019AsoRubin2016 split-GAL4 lines for dopaminergic neurons (AsoRubin2016) | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| FlyLight2019Hampel2015 Grooming neurons and drivers (Hampel 2015) | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| FlyLight2019Klapoetke2017 Split-GAL4 lines from Klapoetke et al. 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| FlyLight2019LateralHorn2019 FlyLight split-GAL4 lines for Lateral Horn | 131 | 131 | 0 | 0 | 0 | 0 | 35 | 0 | -35 (-100.0%) | 82 | 82 | 0 | 0 | 0 | 0 |
| FlyLight2019Namiki2018 split-GAL4 lines for descending neurons (Namiki2018) | 128 | 128 | 0 | 0 | 0 | 0 | 5 | 0 | -5 (-100.0%) | 121 | 121 | 0 | 0 | 0 | 0 |
| FlyLight2019Robie2017 split-GAL4 lines for EB neurons (Robie2017) | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| FlyLight2019Strother2017 Splits targetting the visual motion pathway, Strother2017 | 32 | 32 | 0 | 0 | 0 | 0 | 1 | 0 | -1 (-100.0%) | 31 | 31 | 0 | 0 | 0 | 0 |
| FlyLight2019Wolff2018 Splits targetting CX neurons, Wolff2018 | 21 | 21 | 0 | 0 | 0 | 0 | 8 | 0 | -8 (-100.0%) | 11 | 11 | 0 | 0 | 0 | 0 |
| FlyLight2019Wu2016 split-GAL4 lines for LC VPNs (Wu2016) | 13 | 13 | 0 | 0 | 0 | 0 | 1 | 0 | -1 (-100.0%) | 12 | 12 | 0 | 0 | 0 | 0 |
| FlyLightGen1Set2019 FlyLight - Gen1 GAL4/LexA collection (exported 2019) | 13,587 | 13,587 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 7,968 | 7,967 | -1 (-0.0%) | 0 | 0 | 0 |
| Fushiki2016 Larval peristaltic locomotor system neurons - EM (Fushiki2016) | 82 | 82 | 0 | 82 | 0 | -82 (-100.0%) | 0 | 0 | 0 | 36 | 36 | 0 | 0 | 0 | 0 |
| Gen1MCFODionne2018 MCFO images of GMR-GAL4 lines from Dionne et al., 2018 | 151 | 155 | +4 (+2.6%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Gen1MCFOJenett2012 MCFO images of GMR-GAL4 lines from Jenett et al., 2012 | 15,861 | 19,849 | +3,988 (+25.1%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Gen1MCFOPfeiffer2010 MCFO images of GMR-GAL4 lines from Pfeiffer et al., 2010 | 4 | 10 | +6 (+150.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Gen1MCFOTirian2017 MCFO images of VT-GAL4 lines from Tirian et al., 2017 | 17,149 | 27,940 | +10,791 (+62.9%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Gerhard2017 Nociceptive circuit neurons - EM (Gerhard2017) | 55 | 55 | 0 | 55 | 0 | -55 (-100.0%) | 0 | 0 | 0 | 27 | 27 | 0 | 0 | 0 | 0 |
| Gorko2024 EM FAFB Gorko et al 2024 | 2 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | -2 (-100.0%) | 2 | 2 | 0 | 0 | 0 | 0 |
| Hampel2015 Grooming neurons and drivers (Hampel 2015) | 6 | 6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 3 | 0 | 0 | 0 | 0 |
| Hampel2017 LexA driver targetting mechanosensory eye bristles (Hampel2017) | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| HampelEichler2020 EM FAFB Hampel and Eichler et al 2020 | 147 | 147 | 0 | 0 | 0 | 0 | 28 | 0 | -28 (-100.0%) | 18 | 18 | 0 | 0 | 0 | 0 |
| HeadMusclesMcKellar2020 Images of proboscis muscles from McKellar et al., 2020 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 18 | 18 | 0 | 0 | 0 | 0 |
| Heckscher2015 Eve+ neurons, sensorimotor circuit - EM (Heckscher2015) | 134 | 134 | 0 | 134 | 0 | -134 (-100.0%) | 0 | 0 | 0 | 54 | 54 | 0 | 0 | 0 | 0 |
| Hueckesfeld2020 Unveiling the sensory and interneuronal pathways of the neuroendocrine connectome in Drosophila (Hueckesfeld et al. 2020) | 878 | 878 | 0 | 878 | 0 | -878 (-100.0%) | 0 | 0 | 0 | 113 | 113 | 0 | 0 | 0 | 0 |
| Imambocus2022 EM L1 Imambocus et al., 2022 | 176 | 176 | 0 | 176 | 0 | -176 (-100.0%) | 0 | 0 | 0 | 55 | 55 | 0 | 0 | 0 | 0 |
| Ito2013 Ito lab adult brain lineage clone image set | 96 | 96 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 90 | 90 | 0 | 0 | 0 | 0 |
| JRC2018 JRC 2018 templates & ROIs | 48 | 48 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 48 | 48 | 0 | 0 | 0 | 0 |
| Jenett2012 FlyLight - GMR GAL4 collection (Jenett2012) | 3,469 | 3,469 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3,474 | 3,473 | -1 (-0.0%) | 0 | 0 | 0 |
| JenettShinomya_BrainName BrainName neuropils on adult brain JFRC2 (Jenett, Shinomya) | 58 | 58 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 58 | 58 | 0 | 0 | 0 | 0 |
| Jovanic2016 larval sensorimotor decision pathways (Jovanic2016) | 44 | 44 | 0 | 44 | 0 | -44 (-100.0%) | 0 | 0 | 0 | 25 | 25 | 0 | 0 | 0 | 0 |
| Jovanic2019 EM L1 Jovanic et al. 2019 | 37 | 37 | 0 | 37 | 0 | -37 (-100.0%) | 0 | 0 | 0 | 18 | 18 | 0 | 0 | 0 | 0 |
| Kim2020 EM FAFB Kim et al 2020 | 95 | 95 | 0 | 87 | 0 | -87 (-100.0%) | 0 | 0 | 0 | 8 | 8 | 0 | 0 | 0 | 0 |
| Kind2021 EM FAFB Kind et al. 2021 | 286 | 286 | 0 | 0 | 0 | 0 | 5 | 0 | -5 (-100.0%) | 41 | 41 | 0 | 0 | 0 | 0 |
| Klapoetke2017 Split-GAL4 lines from Klapoetke et al. 2017 | 17 | 92 | +75 (+441.2%) | 0 | 0 | 0 | 3 | 0 | -3 (-100.0%) | 4 | 4 | 0 | 0 | 0 | 0 |
| Knowles_Barley2010 BrainTrap lines (Knowles-Barley2010) | 501 | 501 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 502 | 501 | -1 (-0.2%) | 0 | 0 | 0 |
| Kohl2013 Third order olfactory neurons involved in pheromone response - backfills (Kohl2013) | 111 | 111 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 6 | 6 | 0 | 0 | 0 | 0 |
| Kuan2020 Millimeter-scale imaging of a Drosophila leg at single-neuron resolution | 675 | 675 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 46 | 46 | 0 | 0 | 0 | 0 |
| Larderet2017 larval visual circuit neurons (Larderet2017) | 72 | 72 | 0 | 72 | 0 | -72 (-100.0%) | 0 | 0 | 0 | 12 | 12 | 0 | 0 | 0 | 0 |
| LateralHorn2019 FlyLight split-GAL4 lines for Lateral Horn | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Lee_Lineage2020 central brain neurons by lineage, Lee2020 | 462 | 462 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 38 | 38 | 0 | 0 | 0 | 0 |
| Lillvis2018 Neurons involved in courtship and song (Lillvis2018) | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Mamiya2022 Biomechanical origins of proprioceptive maps in the Drosophila leg | 4 | 4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 3 | 0 | 0 | 0 | 0 |
| Maniates_Selvin2020 EM FANC Phelps et al 2020 | 2,029 | 2,029 | 0 | 1,837 | 0 | -1,837 (-100.0%) | 0 | 0 | 0 | 34 | 34 | 0 | 0 | 0 | 0 |
| Marin2020 EM FAFB Marin et al 2020 | 327 | 327 | 0 | 91 | 0 | -91 (-100.0%) | 91 | 0 | -91 (-100.0%) | 93 | 93 | 0 | 0 | 0 | 0 |
| Mark2019 EM L1 Mark et al. 2019 | 78 | 78 | 0 | 78 | 0 | -78 (-100.0%) | 0 | 0 | 0 | 63 | 63 | 0 | 0 | 0 | 0 |
| Matsuo2016 AMMC local and projection neurons (Matsuo2016) | 41 | 41 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 39 | 39 | 0 | 0 | 0 | 0 |
| McKellar2019 Images of aSP22 descending neuron from McKellar et al., 2019 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| McKellar2020 GAL4 lines from McKellar et al., 2020 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 7 | 6 | -1 (-14.3%) | 0 | 0 | 0 |
| Miroschnikow2018 EM L1 Miroschnikow et al. 2018 | 739 | 739 | 0 | 739 | 0 | -739 (-100.0%) | 0 | 0 | 0 | 79 | 79 | 0 | 0 | 0 | 0 |
| Morimoto2020 EM FAFB Morimoto et al 2020 | 76 | 76 | 0 | 0 | 0 | 0 | 66 | 0 | -66 (-100.0%) | 4 | 4 | 0 | 0 | 0 | 0 |
| Namiki2018 split-GAL4 lines for descending neurons (Namiki2018) | 396 | 5,604 | +5,208 (+1315.2%) | 0 | 0 | 0 | 106 | 0 | -106 (-100.0%) | 134 | 185 | +51 (+38.1%) | 0 | 0 | 0 |
| Nern2024 Optic Lobe connectome neurons from optic_lobe:v1.0.1, Nern et al., 2024 | 53,402 | 53,402 | 0 | 53,400 | 0 | -53,400 (-100.0%) | 0 | 0 | 0 | 844 | 844 | 0 | 0 | 0 | 0 |
| Nern2024roi Optic lobe neuropil ROIs | 105 | 105 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 69 | 69 | 0 | 0 | 0 | 0 |
| Nojima2021 Split-GAL4 lines from Nojima et al., 2021 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 15 | 14 | -1 (-6.7%) | 0 | 0 | 0 |
| Ohyama2015 Neurons involved in larval fast escape response - EM (Ohyama2016) | 109 | 109 | 0 | 108 | 0 | -108 (-100.0%) | 0 | 0 | 0 | 57 | 57 | 0 | 0 | 0 | 0 |
| Ohyama2015roi L1 larval CNS painted domains | 27 | 27 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 14 | 14 | 0 | 0 | 0 | 0 |
| Otto2020 EM FAFB Otto et al 2020 | 807 | 807 | 0 | 12 | 0 | -12 (-100.0%) | 395 | 0 | -395 (-100.0%) | 79 | 79 | 0 | 0 | 0 | 0 |
| Robie2017 split-GAL4 lines for EB neurons (Robie2017) | 84 | 176 | +92 (+109.5%) | 0 | 0 | 0 | 14 | 0 | -14 (-100.0%) | 20 | 20 | 0 | 0 | 0 | 0 |
| Sayin2019 EM FAFB Sayin et al 2019 | 3 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | -3 (-100.0%) | 3 | 3 | 0 | 0 | 0 | 0 |
| Schlegel2016 larval hugin neurons - EM (Schlegel2016) | 193 | 193 | 0 | 192 | 0 | -192 (-100.0%) | 0 | 0 | 0 | 40 | 40 | 0 | 0 | 0 | 0 |
| Shiu2022 EM FAFB Shiu et al. 2022 | 25 | 25 | 0 | 11 | 0 | -11 (-100.0%) | 0 | 0 | 0 | 23 | 23 | 0 | 0 | 0 | 0 |
| SplitAso2014b Split-GAL4 lines from Aso et al., 2014b | 0 | 36 | +36 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitBaker2022 Split-GAL4 lines from Baker et al., 2022 | 16 | 1,741 | +1,725 (+10781.2%) | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 65 | +62 (+2066.7%) | 0 | 0 | 0 |
| SplitBidaye2014 Split-GAL4 lines from Bidaye et al., 2014 | 0 | 73 | +73 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 9 | +9 | 0 | 0 | 0 |
| SplitBidaye2020 Split-GAL4 lines from Bidaye et al., 2020 | 0 | 20 | +20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitBogovic2020 Split-GAL4 lines from Bogovic et al., 2020 | 79 | 217 | +138 (+174.7%) | 0 | 0 | 0 | 0 | 0 | 0 | 9 | 9 | 0 | 0 | 0 | 0 |
| SplitCheong2023 Split-GAL4 lines from Cheong et al., 2023 | 42 | 365 | +323 (+769.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 6 | 18 | +12 (+200.0%) | 0 | 0 | 0 |
| SplitCheong2024 Split-GAL4 lines from Cheong et al., 2024 | 0 | 8 | +8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitDag2019 Split-GAL4 lines from Dag et al., 2019 | 0 | 10 | +10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitDavis2017 Split-GAL4 lines from Turner-Evans et al., 2017 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| SplitDavis2020 Split-GAL4 lines from Davis et al., 2020 | 106 | 775 | +669 (+631.1%) | 0 | 0 | 0 | 82 | 0 | -82 (-100.0%) | 38 | 47 | +9 (+23.7%) | 0 | 0 | 0 |
| SplitEhrhardt2023 Split-GAL4 lines from Ehrhardt et al., 2023 | 117 | 4,667 | +4,550 (+3888.9%) | 0 | 0 | 0 | 0 | 0 | 0 | 41 | 198 | +157 (+382.9%) | 0 | 0 | 0 |
| SplitFeng2014 Split-GAL4 lines from Feng et al., 2014 | 0 | 22 | +22 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitFeng2020 Split-GAL4 lines from Feng et al., 2020 | 35 | 2,012 | +1,977 (+5648.6%) | 0 | 0 | 0 | 0 | 0 | 0 | 7 | 83 | +76 (+1085.7%) | 0 | 0 | 0 |
| SplitGao2019 Split-GAL4 lines from Gao et al., 2019 | 5 | 44 | +39 (+780.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 3 | +1 (+50.0%) | 0 | 0 | 0 |
| SplitGarner2023 Split-GAL4 lines from Garner et al., 2023 | 0 | 120 | +120 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 6 | +6 | 0 | 0 | 0 |
| SplitGiraldo2018 Split-GAL4 lines from Giraldo et al., 2018 | 5 | 34 | +29 (+580.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | +1 (+100.0%) | 0 | 0 | 0 |
| SplitGorko2024 Split-GAL4 lines from Gorko et al., 2024 | 0 | 9 | +9 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | +3 | 0 | 0 | 0 |
| SplitHattori2017 Split-GAL4 lines from Hattori et al., 2017 | 0 | 4 | +4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitHulse2021 Split-GAL4 lines from Hulse et al., 2021 | 0 | 24 | +24 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitIsaacson2023 Split-GAL4 lines from Isaacson et al., 2023 | 8 | 143 | +135 (+1687.5%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 8 | +6 (+300.0%) | 0 | 0 | 0 |
| SplitJovanic2019 Split-GAL4 lines from Jovanic et al., 2019 | 13 | 75 | +62 (+476.9%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 6 | +4 (+200.0%) | 0 | 0 | 0 |
| SplitKind2021 Split-GAL4 lines from Kind et al., 2021 | 13 | 63 | +50 (+384.6%) | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 4 | 0 | 0 | 0 | 0 |
| SplitKlapoetke2022 Split-GAL4 lines from Klapoetke et al., 2022 | 8 | 110 | +102 (+1275.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 4 | 0 | 0 | 0 | 0 |
| SplitLiang2017 Split-GAL4 lines from Liang et al., 2017 | 0 | 2 | +2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitLillvis2022 Split-GAL4 lines from Lillvis et al., 2022 | 0 | 10 | +10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitLillvis2024 Split-GAL4 lines from Lillvis et al., 2024 | 0 | 820 | +820 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 54 | +54 | 0 | 0 | 0 |
| SplitLiu2019 Split-GAL4 lines from Liu et al., 2019 | 0 | 13 | +13 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitLongden2021 Split-GAL4 lines from Longden et al., 2021 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| SplitLongden2023 Split-GAL4 lines from Longden et al., 2023 | 4 | 25 | +21 (+525.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | +1 (+100.0%) | 0 | 0 | 0 |
| SplitMais2021 Split-GAL4 lines from Mais et al., 2021 | 0 | 34 | +34 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitMasek2015 Split-GAL4 lines from Masek et al., 2015 | 6 | 16 | +10 (+166.7%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 |
| SplitMeissner2018 Split-GAL4 lines from Meissner et al., 2018 | 0 | 18 | +18 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitMeissner2024 Split-GAL4 lines from Meissner et al., 2024 | 1,555 | 22,368 | +20,813 (+1338.5%) | 0 | 0 | 0 | 0 | 0 | 0 | 378 | 1,486 | +1,108 (+293.1%) | 0 | 0 | 0 |
| SplitMinegishi2023 Split-GAL4 lines from Minegishi et al., 2023 | 55 | 2,765 | +2,710 (+4927.3%) | 0 | 0 | 0 | 0 | 0 | 0 | 12 | 90 | +78 (+650.0%) | 0 | 0 | 0 |
| SplitMontague2019 Split-GAL4 lines from Montague et al., 2019 | 23 | 43 | +20 (+87.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 4 | +1 (+33.3%) | 0 | 0 | 0 |
| SplitMorimoto2020 Split-GAL4 lines from Morimoto et al., 2020 | 27 | 223 | +196 (+725.9%) | 0 | 0 | 0 | 0 | 0 | 0 | 10 | 11 | +1 (+10.0%) | 0 | 0 | 0 |
| SplitNallasivan2025 Split-GAL4 lines from Nallasivan et al 2025 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| SplitNamiki2022 Split-GAL4 lines from Namiki et al., 2022 | 21 | 458 | +437 (+2081.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 6 | 12 | +6 (+100.0%) | 0 | 0 | 0 |
| SplitNern2025 Split-GAL4 lines from Nern et al., 2025 | 0 | 5,911 | +5,911 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 318 | +318 | 0 | 0 | 0 |
| SplitReyn2017 Split-GAL4 lines from Reyn et al., 2017 | 0 | 35 | +35 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | +3 | 0 | 0 | 0 |
| SplitRibeiro2018 Split-GAL4 lines from Ribeiro et al., 2018 | 0 | 30 | +30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | +3 | 0 | 0 | 0 |
| SplitRubin2024 Split-GAL4 lines from Rubin et al., 2024 | 17 | 226 | +209 (+1229.4%) | 0 | 0 | 0 | 0 | 0 | 0 | 9 | 26 | +17 (+188.9%) | 0 | 0 | 0 |
| SplitSchlichting2019 Split-GAL4 lines from Schlichting et al., 2019 | 4 | 206 | +202 (+5050.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 4 | +3 (+300.0%) | 0 | 0 | 0 |
| SplitSchretter2020 Split-GAL4 lines from Schretter et al., 2020 | 95 | 1,281 | +1,186 (+1248.4%) | 0 | 0 | 0 | 4 | 0 | -4 (-100.0%) | 11 | 13 | +2 (+18.2%) | 0 | 0 | 0 |
| SplitSchretter2024 Split-GAL4 lines from Schretter et al., 2024 | 0 | 9 | +9 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | +3 | 0 | 0 | 0 |
| SplitShao2017 Split-GAL4 lines from Shao et al., 2017 | 0 | 53 | +53 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitShuai2023 Split-GAL4 lines from Shuai et al., 2023 | 4,316 | 8,761 | +4,445 (+103.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 298 | 673 | +375 (+125.8%) | 0 | 0 | 0 |
| SplitSitaraman2015 Split-GAL4 lines from Sitaraman et al., 2015 | 27 | 136 | +109 (+403.7%) | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 7 | +4 (+133.3%) | 0 | 0 | 0 |
| SplitSterne2021 Split-GAL4 lines from Sterne et al., 2021 | 2,082 | 3,989 | +1,907 (+91.6%) | 0 | 0 | 0 | 0 | 0 | 0 | 194 | 264 | +70 (+36.1%) | 0 | 0 | 0 |
| SplitSun2017 Split-GAL4 lines from Sun et al., 2017 | 0 | 20 | +20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitTakagi2017 Split-GAL4 lines from Takagi et al., 2017 | 0 | 2 | +2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitTakemura2017 Split-GAL4 lines from Takemura et al., 2017 | 0 | 30 | +30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitTanaka2008 Split-GAL4 lines from Tanaka et al., 2008 | 0 | 8 | +8 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | +1 | 0 | 0 | 0 |
| SplitTriphan2016 Split-GAL4 lines from Triphan et al., 2016 | 0 | 6 | +6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitTurner_Evans2017 Split-GAL4 lines from Turner-Evans et al., 2017 | 3 | 13 | +10 (+333.3%) | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | +1 (+100.0%) | 0 | 0 | 0 |
| SplitTurner_Evans2020 Split-GAL4 lines from Turner-Evans et al., 2020 | 13 | 110 | +97 (+746.2%) | 0 | 0 | 0 | 4 | 0 | -4 (-100.0%) | 5 | 6 | +1 (+20.0%) | 0 | 0 | 0 |
| SplitTuthill2013 Split-GAL4 lines from Tuthill et al., 2013 | 0 | 239 | +239 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 24 | +24 | 0 | 0 | 0 |
| SplitVijayan2023 Split-GAL4 lines from Vijayan et al., 2023 | 0 | 102 | +102 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 17 | +17 | 0 | 0 | 0 |
| SplitVogt2014 Split-GAL4 lines from Vogt et al., 2014 | 0 | 15 | +15 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitVogt2016 Split-GAL4 lines from Vogt et al., 2016 | 34 | 42 | +8 (+23.5%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 |
| SplitWang2020a Split-GAL4 lines from Wang et al., 2020a | 88 | 427 | +339 (+385.2%) | 0 | 0 | 0 | 16 | 0 | -16 (-100.0%) | 11 | 11 | 0 | 0 | 0 | 0 |
| SplitWang2020b Split-GAL4 lines from Wang et al., 2020b | 15 | 34 | +19 (+126.7%) | 0 | 0 | 0 | 1 | 0 | -1 (-100.0%) | 5 | 6 | +1 (+20.0%) | 0 | 0 | 0 |
| SplitWang2020c Split-GAL4 lines from Wang et al., 2020c | 0 | 156 | +156 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 9 | +9 | 0 | 0 | 0 |
| SplitWolff2025 Split-GAL4 lines from Wolff et al., 2025 | 0 | 2,823 | +2,823 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 231 | +231 | 0 | 0 | 0 |
| SplitXie2021 Split-GAL4 lines from Xie et al., 2021 | 5 | 19 | +14 (+280.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | +2 (+100.0%) | 0 | 0 | 0 |
| SplitYamagata2015 Split-GAL4 lines from Yamagata et al., 2015 | 5 | 11 | +6 (+120.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 |
| SplitYoo2023 Split-GAL4 lines from Yoo et al., 2023 | 0 | 60 | +60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | +4 | 0 | 0 | 0 |
| SplitZhao2023 Split-GAL4 lines from Zhao et al., 2023 | 10 | 29 | +19 (+190.0%) | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 3 | +1 (+50.0%) | 0 | 0 | 0 |
| SplitZhao2025 Split-GAL4 lines from Zhao et al., 2025 | 0 | 16 | +16 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | +2 | 0 | 0 | 0 |
| SplitZung2025 Split-GAL4 lines from Zung et al., 2025 | 0 | 56 | +56 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 20 | +20 | 0 | 0 | 0 |
| Strother2017 Splits targetting the visual motion pathway, Strother2017 | 28 | 148 | +120 (+428.6%) | 0 | 0 | 0 | 11 | 0 | -11 (-100.0%) | 10 | 10 | 0 | 0 | 0 | 0 |
| TaiszGalili2022 EM FAFB Taisz and Galili et al., 2022 | 90 | 90 | 0 | 48 | 0 | -48 (-100.0%) | 15 | 0 | -15 (-100.0%) | 22 | 22 | 0 | 0 | 0 | 0 |
| Takagi2017 Larval wave neurons and circuit partners - EM (Takagi2017) | 38 | 38 | 0 | 38 | 0 | -38 (-100.0%) | 0 | 0 | 0 | 15 | 15 | 0 | 0 | 0 | 0 |
| Takemura2023 Male Adult Nerve Cord (MANC) connectome neurons | 23,759 | 23,759 | 0 | 23,733 | 0 | -23,733 (-100.0%) | 0 | 0 | 0 | 4,063 | 4,063 | 0 | 0 | 0 | 0 |
| Takemura2023roi MANC neuropil and tract ROIs | 59 | 59 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 33 | 33 | 0 | 0 | 0 | 0 |
| Tastekin2018 EM L1 Tastekin et al 2018 | 10 | 10 | 0 | 10 | 0 | -10 (-100.0%) | 0 | 0 | 0 | 5 | 5 | 0 | 0 | 0 | 0 |
| Truman2016 L3 Larval CNS Template (Truman2016) | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| TrumanWood2018 Truman Larval Flip-Out Collection | 12,238 | 12,238 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 |
| TrumanWood2018public Truman Larval Flip-Out Collection | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 1 | -1 (-50.0%) | 0 | 0 | 0 |
| Turner_Evans2020 EM FAFB Turner-Evans et al 2020 | 49 | 49 | 0 | 0 | 0 | 0 | 36 | 0 | -36 (-100.0%) | 17 | 17 | 0 | 0 | 0 | 0 |
| Valdes_Aleman2021 Comparative Connectomics Reveals How Partner Identity, Location, and Activity Specify Synaptic Connectivity in Drosophila (Valdes-Aleman et al. 2021) | 37 | 37 | 0 | 37 | 0 | -37 (-100.0%) | 0 | 0 | 0 | 20 | 20 | 0 | 0 | 0 | 0 |
| Wang2020a EM FAFB Wang et al 2020a | 12 | 12 | 0 | 0 | 0 | 0 | 10 | 0 | -10 (-100.0%) | 10 | 10 | 0 | 0 | 0 | 0 |
| Wang2020b EM FAFB Wang et al 2020b | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Wang2020c EM FAFB Wang et al 2020c | 24 | 24 | 0 | 0 | 0 | 0 | 7 | 0 | -7 (-100.0%) | 9 | 9 | 0 | 0 | 0 | 0 |
| WindingPedigo2023 EM L1 Winding, Pedigo et al., 2023 | 3,066 | 3,066 | 0 | 3,066 | 0 | -3,066 (-100.0%) | 0 | 0 | 0 | 330 | 330 | 0 | 0 | 0 | 0 |
| Wolff2018 Splits targetting CX neurons, Wolff2018 | 265 | 2,156 | +1,891 (+713.6%) | 0 | 0 | 0 | 6 | 0 | -6 (-100.0%) | 91 | 102 | +11 (+12.1%) | 0 | 0 | 0 |
| WoodHartenstein2018 L3 neuropils (WoodHartenstein2018) | 255 | 255 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 138 | 138 | 0 | 0 | 0 | 0 |
| Wu2016 split-GAL4 lines for LC VPNs (Wu2016) | 338 | 2,448 | +2,110 (+624.3%) | 0 | 0 | 0 | 159 | 0 | -159 (-100.0%) | 55 | 60 | +5 (+9.1%) | 0 | 0 | 0 |
| Xie2018 Split GAL4 lines for dopaminergic neurons, Xie2018 | 78 | 78 | 0 | 0 | 0 | 0 | 26 | 0 | -26 (-100.0%) | 70 | 70 | 0 | 0 | 0 | 0 |
| Xu2020Neurons JRC_FlyEM_Hemibrain neurons Version 1.0.1 | 21,242 | 21,242 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 |
| Xu2020NeuronsV1point2point1 JRC_FlyEM_Hemibrain neurons Version 1.2.1 | 22,705 | 22,705 | 0 | 22,432 | 0 | -22,432 (-100.0%) | 9,426 | 0 | -9,426 (-100.0%) | 5,120 | 5,120 | 0 | 0 | 0 | 0 |
| Xu2020roi JRC_FlyEM_Hemibrain painted domains | 219 | 219 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 157 | 157 | 0 | 0 | 0 | 0 |
| Yu2013 Lee lab adult brain lineage clone image set | 95 | 95 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 95 | 95 | 0 | 0 | 0 | 0 |
| Zarin2019 EM L1 Zarin, Mark et al. 2019 | 194 | 194 | 0 | 194 | 0 | -194 (-100.0%) | 0 | 0 | 0 | 87 | 87 | 0 | 0 | 0 | 0 |
| Zhao2023 EM FAFB Zhao et al., 2023 | 1,194 | 1,194 | 0 | 0 | 0 | 0 | 1 | 0 | -1 (-100.0%) | 7 | 7 | 0 | 0 | 0 | 0 |
| Zheng2018 EM FAFB Zheng et al 2018 | 145 | 145 | 0 | 114 | 0 | -114 (-100.0%) | 100 | 0 | -100 (-100.0%) | 71 | 71 | 0 | 0 | 0 | 0 |
| Zheng2020 EM FAFB Zheng et al 2020 (published 2022) | 1,507 | 1,507 | 0 | 23 | 0 | -23 (-100.0%) | 728 | 0 | -728 (-100.0%) | 11 | 11 | 0 | 0 | 0 | 0 |
| Zwart2016 Larval motor circuit neurons (Zwart2016) | 41 | 41 | 0 | 41 | 0 | -41 (-100.0%) | 0 | 0 | 0 | 19 | 19 | 0 | 0 | 0 | 0 |
Node labels and relationship types
| Type | Label | pdb | p3 | Δ |
|---|---|---|---|---|
| node | Acetylcholine_receptor | 13 | 13 | 0 |
| node | Adult | 725,425 | 808,557 | +83,132 (+11.5%) |
| node | Anatomy | 772,943 | 798,239 | +25,296 (+3.3%) |
| node | AnnotationProperty | 344 | 344 | 0 |
| node | API | 8 | 8 | 0 |
| node | Assay | 108 | 108 | 0 |
| node | Auditory_system | 1,777 | 1,777 | 0 |
| node | Calcium_binding | 57 | 75 | +18 (+31.6%) |
| node | Carbohydrate_binding | 42 | 42 | 0 |
| node | Cell | 648,008 | 648,009 | +1 (+0.0%) |
| node | Cell_adhesion | 76 | 76 | 0 |
| node | Channel | 720,562 | 803,659 | +83,097 (+11.5%) |
| node | Chemosensory_system | 19,643 | 19,643 | 0 |
| node | Cholinergic | 313,368 | 313,368 | 0 |
| node | Class | 133,399 | 133,657 | +258 (+0.2%) |
| node | Clone | 308 | 308 | 0 |
| node | Cluster | 3,290 | 3,290 | 0 |
| node | Connectome | 8 | 8 | 0 |
| node | Cytoskeleton_binding | 266 | 287 | +21 (+7.9%) |
| node | DataProperty | 6 | 6 | 0 |
| node | DataSet | 219 | 219 | 0 |
| node | Deprecated | 39,060 | 39,051 | -9 (-0.0%) |
| node | DNA_binding | 813 | 791 | -22 (-2.7%) |
| node | Dopamine_receptor | 4 | 4 | 0 |
| node | Dopaminergic | 20,237 | 20,237 | 0 |
| node | Entity | 1,704,675 | 1,871,198 | +166,523 (+9.8%) |
| node | Enzyme | 3,727 | 3,734 | +7 (+0.2%) |
| node | Expression_pattern | 77,239 | 110,359 | +33,120 (+42.9%) |
| node | Expression_pattern_fragment | 67,074 | 92,399 | +25,325 (+37.8%) |
| node | FAFB | 5,645 | 5,645 | 0 |
| node | FANC | 1,472 | 1,472 | 0 |
| node | Feature | 47,037 | 47,037 | 0 |
| node | FlyCircuit | 16,128 | 16,128 | 0 |
| node | GABA_receptor | 7 | 7 | 0 |
| node | GABAergic | 109,491 | 109,491 | 0 |
| node | Ganglion | 45 | 45 | 0 |
| node | Gene | 17,893 | 17,893 | 0 |
| node | Glial_cell | 256 | 256 | 0 |
| node | Glutamate_receptor | 24 | 24 | 0 |
| node | Glutamatergic | 103,627 | 103,627 | 0 |
| node | GMC | 25 | 25 | 0 |
| node | GPCR | 117 | 120 | +3 (+2.6%) |
| node | Gustatory_receptor | 64 | 64 | 0 |
| node | Gustatory_system | 4,112 | 4,112 | 0 |
| node | has_image | 720,714 | 803,845 | +83,131 (+11.5%) |
| node | has_neuron_connectivity | 491,130 | 461,057 | -30,073 (-6.1%) |
| node | has_region_connectivity | 392,249 | 0 | -392,249 (-100.0%) |
| node | has_subClass | 8,753 | 8,832 | +79 (+0.9%) |
| node | hasScRNAseq | 13,388 | 626 | -12,762 (-95.3%) |
| node | Histamine_receptor | 2 | 2 | 0 |
| node | Histaminergic | 24,512 | 24,512 | 0 |
| node | Hormone | 21 | 23 | +2 (+9.5%) |
| node | Hygrosensory_system | 579 | 579 | 0 |
| node | Individual | 1,570,537 | 1,736,802 | +166,265 (+10.6%) |
| node | Ion_channel | 396 | 395 | -1 (-0.3%) |
| node | L1EM | 5,051 | 5,051 | 0 |
| node | Larva | 23,420 | 23,439 | +19 (+0.1%) |
| node | License | 8 | 8 | 0 |
| node | Ligand | 119 | 119 | 0 |
| node | lineage_0_MNB | 1,190 | 1,190 | 0 |
| node | lineage_10_NB2-2 | 0 | 1,484 | +1,484 |
| node | lineage_11_NB7-2 | 0 | 1,205 | +1,205 |
| node | lineage_12_NB6-1 | 0 | 2,935 | +2,935 |
| node | lineage_13_NB4-2 | 0 | 2,925 | +2,925 |
| node | lineage_14_NB4-1 | 0 | 1,909 | +1,909 |
| node | lineage_15_NB2-3 | 0 | 571 | +571 |
| node | lineage_16_NB1-1 | 0 | 1,745 | +1,745 |
| node | lineage_17_NB2-5 | 0 | 1,525 | +1,525 |
| node | lineage_18_NB2-4 | 0 | 705 | +705 |
| node | lineage_19_NB6-2 | 0 | 3,747 | +3,747 |
| node | lineage_1_NB1-2 | 0 | 3,132 | +3,132 |
| node | lineage_20_NB5-7 | 0 | 5 | +5 |
| node | lineage_21_NB4-3 | 0 | 1,439 | +1,439 |
| node | lineage_22_NB5-4 | 0 | 12 | +12 |
| node | lineage_23_NB7-4 | 0 | 1,572 | +1,572 |
| node | lineage_24_NB4-4 | 0 | 25 | +25 |
| node | lineage_25_NB3-4 | 0 | 9 | +9 |
| node | lineage_26_NB5-1 | 0 | 66 | +66 |
| node | lineage_2_NB2-1 | 0 | 1,099 | +1,099 |
| node | lineage_3_NB7-1 | 0 | 3,677 | +3,677 |
| node | lineage_4_NB3-1 | 0 | 1,885 | +1,885 |
| node | lineage_5_NB5-3 | 0 | 1,357 | +1,357 |
| node | lineage_6_NB5-2 | 0 | 3,696 | +3,696 |
| node | lineage_7_NB3-2 | 0 | 2,469 | +2,469 |
| node | lineage_8_NB3-3 | 0 | 2,838 | +2,838 |
| node | lineage_9_NB3-5 | 0 | 2,663 | +2,663 |
| node | lineage_ALad1_BAmv3 | 1,314 | 1,314 | 0 |
| node | lineage_ALl1_BAlc | 2,818 | 2,818 | 0 |
| node | lineage_ALlv1_BAlp4 | 735 | 735 | 0 |
| node | lineage_ALv1_BAla1 | 1,217 | 1,217 | 0 |
| node | lineage_ALv2_BAla2 | 695 | 695 | 0 |
| node | lineage_AOTUv1_DALcm2 | 702 | 702 | 0 |
| node | lineage_AOTUv2_DALl1 | 398 | 398 | 0 |
| node | lineage_AOTUv3_DALcl1 | 1,488 | 1,488 | 0 |
| node | lineage_AOTUv4_DALcl2 | 1,421 | 1,421 | 0 |
| node | lineage_BLAd4 | 2 | 2 | 0 |
| node | lineage_BLP3 | 18 | 18 | 0 |
| node | lineage_BLP5 | 2 | 2 | 0 |
| node | lineage_BLVa3 | 2 | 2 | 0 |
| node | lineage_BLVa4 | 2 | 2 | 0 |
| node | lineage_CLp1_DPLc4 | 549 | 549 | 0 |
| node | lineage_CLp2_CP4 | 299 | 299 | 0 |
| node | lineage_CM2 | 2 | 2 | 0 |
| node | lineage_CREa1_BAmd1 | 1,024 | 1,024 | 0 |
| node | lineage_CREa2_DALcm1 | 1,351 | 1,351 | 0 |
| node | lineage_CREl1_DALv3 | 500 | 500 | 0 |
| node | lineage_DAMd2 | 2 | 2 | 0 |
| node | lineage_DAMd3 | 2 | 2 | 0 |
| node | lineage_DAMv1 | 2 | 2 | 0 |
| node | lineage_DAMv2 | 2 | 2 | 0 |
| node | lineage_DL1_CP2 | 2,580 | 2,580 | 0 |
| node | lineage_DL2_CP3 | 1,106 | 1,106 | 0 |
| node | lineage_DM1_DPMm1 | 2,915 | 2,915 | 0 |
| node | lineage_DM2_DPMpm1 | 1,998 | 1,998 | 0 |
| node | lineage_DM3_DPMpm2 | 2,340 | 2,340 | 0 |
| node | lineage_DM4_CM4 | 3,519 | 3,519 | 0 |
| node | lineage_DM5_CM1 | 757 | 757 | 0 |
| node | lineage_DM6_CM3 | 3,742 | 3,742 | 0 |
| node | lineage_DPLcv | 2 | 2 | 0 |
| node | lineage_DPMm3 | 2 | 2 | 0 |
| node | lineage_EBa1_DALv2 | 1,725 | 1,725 | 0 |
| node | lineage_FLAa1_BAla4 | 98 | 98 | 0 |
| node | lineage_FLAa2_BAmas1 | 701 | 701 | 0 |
| node | lineage_FLAa3_BAmas2 | 422 | 422 | 0 |
| node | lineage_LALa1_BAlp2 | 1,237 | 1,237 | 0 |
| node | lineage_LALv1_BAmv1 | 1,427 | 1,427 | 0 |
| node | lineage_LHa1_BLAd1 | 545 | 545 | 0 |
| node | lineage_LHa2_BLVa1 | 633 | 633 | 0 |
| node | lineage_LHa3_BLVa2 | 547 | 547 | 0 |
| node | lineage_LHa4 | 4 | 4 | 0 |
| node | lineage_LHd1_DPLd | 500 | 500 | 0 |
| node | lineage_LHd2_DPLm2 | 628 | 628 | 0 |
| node | lineage_LHl1_BLD4 | 841 | 841 | 0 |
| node | lineage_LHl2_DPLal2 | 916 | 916 | 0 |
| node | lineage_LHl3_BLVa2b | 137 | 137 | 0 |
| node | lineage_LHl4_BLD1 | 1,398 | 1,398 | 0 |
| node | lineage_LHp1_BLP4 | 808 | 808 | 0 |
| node | lineage_LHp2_DPLp1 | 1,224 | 1,224 | 0 |
| node | lineage_LHp3_CP5 | 233 | 233 | 0 |
| node | lineage_MBp | 19,312 | 19,312 | 0 |
| node | lineage_MBp1 | 2,332 | 2,332 | 0 |
| node | lineage_MBp2 | 2,314 | 2,314 | 0 |
| node | lineage_MBp3 | 2,344 | 2,344 | 0 |
| node | lineage_MBp4 | 2,391 | 2,391 | 0 |
| node | lineage_NB1-3 | 0 | 13 | +13 |
| node | lineage_NB5-5 | 0 | 2 | +2 |
| node | lineage_NB5-6 | 0 | 31 | +31 |
| node | lineage_NB6-4 | 0 | 15 | +15 |
| node | lineage_NB7-3 | 0 | 27 | +27 |
| node | lineage_PBp1_CM6 | 298 | 298 | 0 |
| node | lineage_PSa1_BAmv2 | 580 | 580 | 0 |
| node | lineage_PSp1_DPMl2 | 243 | 243 | 0 |
| node | lineage_PSp2_CM5 | 543 | 543 | 0 |
| node | lineage_PSp3_DPMl1 | 731 | 731 | 0 |
| node | lineage_SIPa1_BLAd2 | 677 | 677 | 0 |
| node | lineage_SIPp1_DPMpl2 | 334 | 334 | 0 |
| node | lineage_SLPa&l1_BLAvm | 0 | 1,566 | +1,566 |
| node | lineage_SLPad1_DPLl3 | 1,263 | 1,263 | 0 |
| node | lineage_SLPal1_DPLal1 | 679 | 679 | 0 |
| node | lineage_SLPal2_DPLal3 | 610 | 610 | 0 |
| node | lineage_SLPal3_BLAd3 | 6 | 6 | 0 |
| node | lineage_SLPal4 | 4 | 4 | 0 |
| node | lineage_SLPal5_BLAd5 | 325 | 325 | 0 |
| node | lineage_SLPav1_BLAl1 | 705 | 705 | 0 |
| node | lineage_SLPav2_BLD2 | 681 | 681 | 0 |
| node | lineage_SLPav3_BLVa2a | 327 | 327 | 0 |
| node | lineage_SLPp&v1_DPLp2 | 0 | 608 | +608 |
| node | lineage_SLPpl1_DPLl1 | 886 | 886 | 0 |
| node | lineage_SLPpl2_CP6 | 327 | 327 | 0 |
| node | lineage_SLPpl3_BLVa2c | 438 | 438 | 0 |
| node | lineage_SLPpm1_DPLm1 | 601 | 601 | 0 |
| node | lineage_SLPpm2_DPLc2 | 253 | 253 | 0 |
| node | lineage_SLPpm3_DPLc3 | 421 | 421 | 0 |
| node | lineage_SLPpm4 | 12 | 12 | 0 |
| node | lineage_SMPad1 | 761 | 761 | 0 |
| node | lineage_SMPad2 | 1,189 | 1,189 | 0 |
| node | lineage_SMPad3_DAMd1 | 593 | 593 | 0 |
| node | lineage_SMPad4 | 7 | 7 | 0 |
| node | lineage_SMPp&v1_DPLc5 | 0 | 923 | +923 |
| node | lineage_SMPpd1_DPLc1 | 652 | 652 | 0 |
| node | lineage_SMPpd2_DPLc6 | 151 | 151 | 0 |
| node | lineage_SMPpm1_DPMm2 | 441 | 441 | 0 |
| node | lineage_SMPpv1_DPMpl1 | 509 | 509 | 0 |
| node | lineage_SMPpv2_CP1 | 780 | 780 | 0 |
| node | lineage_TRco | 2 | 2 | 0 |
| node | lineage_TRdl | 657 | 657 | 0 |
| node | lineage_TRdm | 546 | 546 | 0 |
| node | lineage_TRvl | 2 | 2 | 0 |
| node | lineage_TRvm | 2 | 2 | 0 |
| node | lineage_VESa1_BAla3 | 276 | 276 | 0 |
| node | lineage_VESa2_BAlp1 | 279 | 279 | 0 |
| node | lineage_VLPa1_DALl2 | 966 | 966 | 0 |
| node | lineage_VLPa2_DALv1 | 968 | 968 | 0 |
| node | lineage_VLPd&p1_DPLl2 | 0 | 1,191 | +1,191 |
| node | lineage_VLPd1_DPLam | 542 | 542 | 0 |
| node | lineage_VLPl&d1_BLAv1 | 0 | 1,426 | +1,426 |
| node | lineage_VLPl&p1_BLVp2 | 0 | 1,386 | +1,386 |
| node | lineage_VLPl&p2_BLVp1 | 0 | 1,986 | +1,986 |
| node | lineage_VLPl1 | 5 | 5 | 0 |
| node | lineage_VLPl2_BLAv2 | 1,961 | 1,961 | 0 |
| node | lineage_VLPl4_BLD3 | 746 | 746 | 0 |
| node | lineage_VLPp&l1_DPLpv | 0 | 1,677 | +1,677 |
| node | lineage_VLPp1_BLP2 | 479 | 479 | 0 |
| node | lineage_VLPp2_DPMpl3 | 450 | 450 | 0 |
| node | lineage_VPNd1_BLD6 | 1,905 | 1,905 | 0 |
| node | lineage_VPNd2 | 2,850 | 2,850 | 0 |
| node | lineage_VPNd3 | 1,079 | 1,079 | 0 |
| node | lineage_VPNd4 | 4 | 4 | 0 |
| node | lineage_VPNl&d1_BLAl2 | 0 | 879 | +879 |
| node | lineage_VPNp&v1_BLP1 | 0 | 1,999 | +1,999 |
| node | lineage_VPNp1_BLD5 | 793 | 793 | 0 |
| node | lineage_VPNp2 | 652 | 652 | 0 |
| node | lineage_VPNp3 | 942 | 942 | 0 |
| node | lineage_VPNv1 | 1,146 | 1,146 | 0 |
| node | lineage_VPNv2 | 634 | 634 | 0 |
| node | lineage_VPNv3 | 4 | 4 | 0 |
| node | lineage_WEDa1_BAlv | 633 | 633 | 0 |
| node | lineage_WEDa2_BAlp3 | 810 | 810 | 0 |
| node | lineage_WEDd1_DALd | 795 | 795 | 0 |
| node | lineage_WEDd2_BAmd2 | 287 | 287 | 0 |
| node | Lipid_binding | 131 | 147 | +16 (+12.2%) |
| node | Mechanosensory_ion_channel | 11 | 11 | 0 |
| node | Mechanosensory_system | 23,423 | 23,423 | 0 |
| node | Metal_ion_binding | 141 | 162 | +21 (+14.9%) |
| node | Motor_neuron | 4,639 | 4,639 | 0 |
| node | Muscle | 1,941 | 1,941 | 0 |
| node | NBLAST | 450,640 | 0 | -450,640 (-100.0%) |
| node | NBLASTexp | 18,411 | 0 | -18,411 (-100.0%) |
| node | Nervous_system | 738,058 | 821,175 | +83,117 (+11.3%) |
| node | Neuroblast | 518 | 518 | 0 |
| node | Neuromere | 108 | 108 | 0 |
| node | Neuron | 645,495 | 645,496 | +1 (+0.0%) |
| node | Neuron_projection_bundle | 811 | 811 | 0 |
| node | neuronbridge | 44,696 | 0 | -44,696 (-100.0%) |
| node | Neuropeptide | 50 | 50 | 0 |
| node | Neurotransmitter_receptor | 45 | 37 | -8 (-17.8%) |
| node | Nociceptive_system | 351 | 351 | 0 |
| node | ObjectProperty | 388 | 388 | 0 |
| node | Octopamine_receptor | 7 | 7 | 0 |
| node | Octopaminergic | 680 | 680 | 0 |
| node | Odorant_binding | 56 | 56 | 0 |
| node | Olfactory_receptor | 65 | 65 | 0 |
| node | Olfactory_system | 13,238 | 13,238 | 0 |
| node | Peptide_or_protein_hormone_receptor | 71 | 71 | 0 |
| node | Peptidergic | 20,177 | 20,177 | 0 |
| node | Person | 6 | 6 | 0 |
| node | Photoreceptor | 12 | 12 | 0 |
| node | preferred_root | 5 | 5 | 0 |
| node | primary_neuron | 24,497 | 24,500 | +3 (+0.0%) |
| node | Property | 737 | 737 | 0 |
| node | Proprioceptive_system | 3,134 | 3,134 | 0 |
| node | pub | 5,849 | 5,917 | +68 (+1.2%) |
| node | Receptor | 591 | 592 | +1 (+0.2%) |
| node | Regulator | 518 | 552 | +34 (+6.6%) |
| node | RNA_binding | 360 | 490 | +130 (+36.1%) |
| node | Sample | 350 | 350 | 0 |
| node | scRNAseq_DataSet | 24 | 24 | 0 |
| node | secondary_neuron | 186,604 | 186,604 | 0 |
| node | Sense_organ | 931 | 931 | 0 |
| node | Sensory_neuron | 69,711 | 69,712 | +1 (+0.0%) |
| node | Serotonergic | 2,685 | 2,685 | 0 |
| node | Serotonin_receptor | 5 | 5 | 0 |
| node | Site | 46 | 47 | +1 (+2.2%) |
| node | Small_molecule_binding | 391 | 434 | +43 (+11.0%) |
| node | Split | 16,485 | 49,605 | +33,120 (+200.9%) |
| node | Stage | 222 | 222 | 0 |
| node | Structural_molecule | 345 | 409 | +64 (+18.6%) |
| node | Synaptic_neuropil | 1,794 | 1,794 | 0 |
| node | Synaptic_neuropil_block | 45 | 45 | 0 |
| node | Synaptic_neuropil_domain | 633 | 633 | 0 |
| node | Synaptic_neuropil_subdomain | 1,113 | 1,113 | 0 |
| node | Template | 20 | 20 | 0 |
| node | Thermosensory_ion_channel | 1 | 1 | 0 |
| node | Thermosensory_system | 540 | 540 | 0 |
| node | Transcription_factor | 812 | 810 | -2 (-0.2%) |
| node | Transporter | 728 | 736 | +8 (+1.1%) |
| node | Tyramine_receptor | 4 | 4 | 0 |
| node | Tyraminergic | 176 | 176 | 0 |
| node | UnknownType | 11 | 11 | 0 |
| node | VFB | 1,439,515 | 1,605,709 | +166,194 (+11.5%) |
| node | Visual_system | 352,466 | 352,466 | 0 |
| relationship | achieves_planned_objective | 8 | 8 | 0 |
| relationship | adjacent_to | 15 | 15 | 0 |
| relationship | attached_to | 189 | 189 | 0 |
| relationship | attached_to_part_of | 36 | 36 | 0 |
| relationship | bearer_of | 5,047 | 5,047 | 0 |
| relationship | bounding_layer_of | 1 | 1 | 0 |
| relationship | capable_of | 303,250 | 303,250 | 0 |
| relationship | capable_of_part_of | 608 | 608 | 0 |
| relationship | causal_agent_in_process | 1 | 1 | 0 |
| relationship | completely_varies_with | 1 | 1 | 0 |
| relationship | composed_primarily_of | 3,346 | 3,346 | 0 |
| relationship | concretizes | 1 | 1 | 0 |
| relationship | connected_to | 2 | 2 | 0 |
| relationship | consider | 629 | 628 | -1 (-0.2%) |
| relationship | contains | 3 | 3 | 0 |
| relationship | contains_process | 2 | 2 | 0 |
| relationship | continuous_with | 546 | 545 | -1 (-0.2%) |
| relationship | contributes_to | 419 | 447 | +28 (+6.7%) |
| relationship | contributes_to_morphology_of | 1 | 1 | 0 |
| relationship | contributor | 862,368 | 945,498 | +83,130 (+9.6%) |
| relationship | created_by | 34 | 33 | -1 (-2.9%) |
| relationship | creator | 7 | 7 | 0 |
| relationship | database_cross_reference | 1,717,296 | 1,994,299 | +277,003 (+16.1%) |
| relationship | decreased_in_magnitude_relative_to | 1 | 1 | 0 |
| relationship | depicts | 720,560 | 803,657 | +83,097 (+11.5%) |
| relationship | derives_from | 65 | 65 | 0 |
| relationship | determined_by | 15 | 15 | 0 |
| relationship | determined_by_part_of | 355 | 355 | 0 |
| relationship | develops_directly_from | 18 | 18 | 0 |
| relationship | develops_from | 138,852 | 138,854 | +2 (+0.0%) |
| relationship | develops_from_part_of | 7 | 7 | 0 |
| relationship | develops_into | 533 | 534 | +1 (+0.2%) |
| relationship | electrically_synapsed_to | 30 | 30 | 0 |
| relationship | enables | 13,484 | 14,940 | +1,456 (+10.8%) |
| relationship | ends | 2 | 2 | 0 |
| relationship | ends_with | 1 | 1 | 0 |
| relationship | existence_ends_during | 4,130 | 4,130 | 0 |
| relationship | existence_ends_during_or_before | 1 | 1 | 0 |
| relationship | existence_ends_with | 2 | 2 | 0 |
| relationship | existence_overlaps | 115,653 | 115,653 | 0 |
| relationship | existence_starts_during | 4,122 | 4,122 | 0 |
| relationship | existence_starts_during_or_after | 1 | 1 | 0 |
| relationship | existence_starts_with | 3 | 3 | 0 |
| relationship | expresses | 7,059,288 | 71,650 | -6,987,638 (-99.0%) |
| relationship | fasciculates_with | 55,270 | 55,270 | 0 |
| relationship | formed_as_result_of | 7 | 7 | 0 |
| relationship | guided_by | 1 | 1 | 0 |
| relationship | happens_during | 1 | 1 | 0 |
| relationship | has_2D_boundary | 1 | 1 | 0 |
| relationship | has_assay_method | 108 | 108 | 0 |
| relationship | has_component | 2 | 2 | 0 |
| relationship | has_cross_section | 2 | 2 | 0 |
| relationship | has_curation_status | 401 | 401 | 0 |
| relationship | has_disposition | 1 | 1 | 0 |
| relationship | has_fasciculating_neuron_projection | 233 | 233 | 0 |
| relationship | has_habitat | 1 | 1 | 0 |
| relationship | has_hemidriver | 15,637 | 15,637 | 0 |
| relationship | has_increased_levels_of | 5 | 5 | 0 |
| relationship | has_input | 117 | 117 | 0 |
| relationship | has_license | 219 | 219 | 0 |
| relationship | has_location | 2 | 2 | 0 |
| relationship | has_member | 7 | 7 | 0 |
| relationship | has_obsolescence_reason | 461 | 461 | 0 |
| relationship | has_origin | 29 | 29 | 0 |
| relationship | has_output | 12 | 12 | 0 |
| relationship | has_part | 19,249 | 19,248 | -1 (-0.0%) |
| relationship | has_participant | 11 | 11 | 0 |
| relationship | has_postsynaptic_terminal_in | 2,788,256 | 0 | -2,788,256 (-100.0%) |
| relationship | has_potential_to_develop_into | 3 | 3 | 0 |
| relationship | has_presynaptic_terminals_in | 2,273,637 | 0 | -2,273,637 (-100.0%) |
| relationship | has_quality | 170 | 170 | 0 |
| relationship | has_reference | 479,524 | 517,156 | +37,632 (+7.8%) |
| relationship | has_role | 52 | 105 | +53 (+101.9%) |
| relationship | has_scope | 2 | 2 | 0 |
| relationship | has_sensory_dendrite_in | 692 | 692 | 0 |
| relationship | has_sequence | 2 | 2 | 0 |
| relationship | has_sequence_attribute | 2 | 2 | 0 |
| relationship | has_sequence_feature | 3 | 3 | 0 |
| relationship | has_similar_morphology_to | 47,501,032 | 0 | -47,501,032 (-100.0%) |
| relationship | has_similar_morphology_to_part_of | 664,699 | 0 | -664,699 (-100.0%) |
| relationship | has_soma_location | 549,961 | 549,961 | 0 |
| relationship | has_source | 960,297 | 1,043,394 | +83,097 (+8.7%) |
| relationship | has_specified_input | 3 | 3 | 0 |
| relationship | has_specified_output | 3 | 3 | 0 |
| relationship | has_subsequence | 1 | 1 | 0 |
| relationship | has_synaptic_IO_in_region | 2,269 | 2,269 | 0 |
| relationship | has_synaptic_IO_throughout | 13 | 13 | 0 |
| relationship | has_variant_part | 1 | 1 | 0 |
| relationship | immediate_transformation_of | 1 | 1 | 0 |
| relationship | immediately_preceded_by | 250 | 250 | 0 |
| relationship | immediately_precedes | 20 | 20 | 0 |
| relationship | in_register_with | 869,271 | 952,368 | +83,097 (+9.6%) |
| relationship | in_subset | 11,215 | 11,219 | +4 (+0.0%) |
| relationship | in_taxon | 4 | 4 | 0 |
| relationship | increased_in_magnitude_relative_to | 1 | 1 | 0 |
| relationship | inheres_in | 14 | 14 | 0 |
| relationship | innervated_by | 17 | 17 | 0 |
| relationship | innervates | 298 | 298 | 0 |
| relationship | input_of | 108 | 108 | 0 |
| relationship | INSTANCEOF | 2,584,380 | 2,773,392 | +189,012 (+7.3%) |
| relationship | is_about | 12 | 12 | 0 |
| relationship | is_allele_of | 18,150 | 18,150 | 0 |
| relationship | is_deprotonated_form_of | 7 | 7 | 0 |
| relationship | is_direct_form_of | 5 | 5 | 0 |
| relationship | is_homeomorphic_for | 7 | 7 | 0 |
| relationship | is_indirect_form_of | 2 | 2 | 0 |
| relationship | is_negative_form_of | 7 | 7 | 0 |
| relationship | is_opposite_of | 2 | 2 | 0 |
| relationship | is_part_of | 3,811 | 3,811 | 0 |
| relationship | is_positive_form_of | 7 | 7 | 0 |
| relationship | is_proper_part_of | 1 | 1 | 0 |
| relationship | is_protonated_form_of | 7 | 7 | 0 |
| relationship | is_sequence_of | 1 | 1 | 0 |
| relationship | is_specified_output_of | 720,587 | 803,684 | +83,097 (+11.5%) |
| relationship | is_subsequence_of | 2 | 2 | 0 |
| relationship | is_variant_allele_of | 1 | 1 | 0 |
| relationship | located_in | 6 | 6 | 0 |
| relationship | makes_use_of | 49 | 49 | 0 |
| relationship | may_be_identical_to | 250 | 250 | 0 |
| relationship | member_of | 2 | 2 | 0 |
| relationship | negatively_regulates | 400 | 399 | -1 (-0.2%) |
| relationship | never_in_taxon | 5 | 5 | 0 |
| relationship | non_functional_homolog_of | 4 | 4 | 0 |
| relationship | occurs_in | 48 | 48 | 0 |
| relationship | only_in_taxon | 8 | 8 | 0 |
| relationship | output_of | 3 | 3 | 0 |
| relationship | overlaps | 557,214 | 557,224 | +10 (+0.0%) |
| relationship | part_of | 1,052,449 | 1,268,715 | +216,266 (+20.5%) |
| relationship | partially_surrounded_by | 1 | 1 | 0 |
| relationship | participates_in | 1 | 1 | 0 |
| relationship | positively_regulates | 410 | 409 | -1 (-0.2%) |
| relationship | preceded_by | 6 | 6 | 0 |
| relationship | precedes | 3 | 3 | 0 |
| relationship | present_in_taxon | 54 | 54 | 0 |
| relationship | process_has_causal_agent | 4 | 4 | 0 |
| relationship | produced_by | 2 | 2 | 0 |
| relationship | produces | 1 | 1 | 0 |
| relationship | receives_input_from | 94 | 94 | 0 |
| relationship | receives_synaptic_input_from_neuron | 813 | 813 | 0 |
| relationship | receives_synaptic_input_in_region | 26,035 | 26,039 | +4 (+0.0%) |
| relationship | receives_synaptic_input_throughout | 612 | 612 | 0 |
| relationship | reciprocal_of | 1 | 1 | 0 |
| relationship | regulates | 433 | 434 | +1 (+0.2%) |
| relationship | results_in_formation_of_anatomical_entity | 2 | 2 | 0 |
| relationship | sends_synaptic_output_throughout | 127 | 127 | 0 |
| relationship | sends_synaptic_output_to_cell | 847 | 847 | 0 |
| relationship | sends_synaptic_output_to_region | 23,223 | 23,234 | +11 (+0.0%) |
| relationship | sequence_role | 2 | 2 | 0 |
| relationship | simultaneous_with | 6 | 6 | 0 |
| relationship | starts | 1 | 1 | 0 |
| relationship | SUBCLASSOF | 188,817 | 206,687 | +17,870 (+9.5%) |
| relationship | substage_of | 196 | 196 | 0 |
| relationship | surrounded_by | 4 | 4 | 0 |
| relationship | synapsed_to | 35,190,803 | 31,691,089 | -3,499,714 (-9.9%) |
| relationship | synapsed_via_type_Ib_bouton_to | 217 | 217 | 0 |
| relationship | synapsed_via_type_II_bouton_to | 17 | 17 | 0 |
| relationship | synapsed_via_type_III_bouton_to | 14 | 14 | 0 |
| relationship | synapsed_via_type_Is_bouton_to | 1 | 1 | 0 |
| relationship | synapses_restricted_to_region | 34 | 34 | 0 |
| relationship | temporal_interpretation | 40 | 40 | 0 |
| relationship | term_editor | 177 | 177 | 0 |
| relationship | term_replaced_by | 20,782 | 20,778 | -4 (-0.0%) |
| relationship | transcribed_from | 1 | 1 | 0 |
| relationship | transcribed_to | 7 | 7 | 0 |
| relationship | variant_of | 3 | 3 | 0 |
| relationship | varies_with | 2 | 2 | 0 |
Downloads
VFB_reporting format: pdb_report.tsv · p3_report.tsv · pdb_p3_diff.tsv · pdb_label_count_report.tsv · p3_label_count_report.tsv