CS202210140_263
MGE_262 (CS202210140_263)
Hierarchy: CS202210140_484 > CS202210140_263
PURL: https://purl.brain-bican.org/taxonomy/CS202210140/CS202210140_neurons/CS202210140_263
Labelset: Cluster (Rank: 1)
Parent Cell Set: MGE interneuron (CS202210140_484)
Cell Ontology Term: pvalb GABAergic cortical interneuron (CL:4023018)
Rationale DOIs |
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https://doi.org/10.1038/s41586-020-2781-z |
Marker Genes |
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FOXG1 |
NR2F1 |
DLX1 |
LHX6 |
GAD2 |
PVALB |
Transferred annotations:
Transferred cell label | Source taxonomy | Source node accession | Algorithm name | Comment |
---|---|---|---|---|
Pvalb | https://purl.brain-bican.org/taxonomy/AIT_MTG/AIT_MTG.json | CrossArea_subclass:5bcef2988c | We performed PCA (50 components) on our full dataset, trained a random forest classifier (scikit-learn, class_ weight=‘balanced’, max_depth=50) on the MTG labels, and then predicted labels for all cells. We labeled each cluster with the mode of its constituent cells if two conditions were met: more than 0.8 of predicted labels matched the mode, and the mean probability of these pre- dictions was greater than 0.8. |
Author annotation fields:
Author annotation | Value |
---|---|
Cluster ID | 262 |
Class auto_annotation | NEUR |
Neurotransmitter auto_annotation | GABA |
Neuropeptide auto_annotation | CCK CHGA CHGB CORT IGF NAMPT NMU NPPC NUCB NXPH PNOC SCG TAC UBL VGF proSAAS |
Subtype auto_annotation | INT-PVALB |
Transferred MTG Label | Pvalb |
Top three regions | Cerebral cortex: 94.5%, Basal forebrain: 2.1%, Hippocampus: 1.8% |
Top three dissections | Human M1C: 8.7%, Human MTG: 7.9%, Human A29-A30: 4.5% |
Top Enriched Genes | RNF144B, AL136114.1, PRDM1, SULF1, LRRC38, TCIM, WNT16, MYO5B, KCNS3, AL096865.1 |
Number of cells | 10119.0 |
DoubletFinder score | 0.01864453 |
Total UMI | 16405.69206 |
Fraction unspliced | 0.698203376 |
Fraction mitochondrial | 0.011458744 |
H19.30.002 | 3248.0 |
H19.30.001 | 3195.0 |
H18.30.002 | 3183.0 |
H18.30.001 | 493.0 |
Fraction cells from top donor | 0.320980334 |
Number of donors | 4.0 |
subcluster_id | None |