LUSC-092-18-1A
De-identified Human Immune Atlas donor/sample detail for CancerSCEM 2.0. The record preserves available public metadata while avoiding direct identifiers.
Donor-Level Analysis Results
No matrix-backed donor-level analysis package is currently available for LUSC-092-18-1A.
This CancerSCEM record is present in the donor manifest, but the current web analysis layer does not have a readable matrix plus UMAP pair for this donor. The donor metadata and any available UMAP preview remain shown on this page.
Primary Metadata
Core de-identified metadata fields migrated from the ImmuneAging donor manifest.
Donor ID
LUSC-092-18-1A
Sample ID
LUSC-092-18-1A
Dataset
CancerSCEM 2.0
Cohort
CancerSCEM 2.0 Chinese subset; Lung Squamous Cell Carcinoma
Age / Age Group
Pan-cancer Chinese cohort, per-donor ages not in CancerSCEM metadata
Sex
Not reported in public CancerSCEM metadata
Health Status
Lung Squamous Cell Carcinoma; Tumour
Tissue / Cell Source
Tumour
Modality
scRNA-seq (10X Genomics)
Cell Count
Pending
Analysis Status
Matrix pending
UMAP Status
Not generated
Metadata / Source Notes
Project ID: LUSC-092; Cancer type: Lung Squamous Cell Carcinoma; Source: NCBI (SRA); Accession: PRJNA976462; Country: CHN; Sample type: Tumour; Protocol: 10X Genomics; Matrix: pending download; Age/sex not reported in public CancerSCEM metadata. Age source: CancerSCEM 2.0 database; 400 samples across 47 cancer types; donor-level age not included in download.csv
Additional Clinical / Source Fields
Supplementary source metadata retained from the migrated manifest where available.
cancer type
Lung Squamous Cell Carcinoma
cancer type short
LUSC
library count
1
library sample ids
LUSC-092-18-1A
source reference
CancerSCEM 2.0 metadata table; data source=NCBI (SRA); accession=PRJNA976462; downloaded 2026-07-06
data accession
PRJNA976462
project id
LUSC-092
sample type
Tumour
country
CHN
data source
NCBI (SRA)
accession no
PRJNA976462
construction protocol
10X Genomics
transcriptome profile
Yes
metabolic profile
Yes
matrix status
Matrix pending