Journal: Scientific Reports

Article Title: A simplified preparation method for single-nucleus RNA-sequencing using long-term frozen brain tumor tissues

doi: 10.1038/s41598-025-97053-9

Figure Lengend Snippet: Comparison of platforms for studying tumor heterogeneity using patient-derived xenografts. ( a ) Variance between the numbers of human and mouse transcripts per nuclei from 10X snRNA- seq data of a glioma PDX sample. ( b ) Number of genes per cell and ( c ) gene expression levels between 10X and C1 platforms. ( d ) Comparison to bulk PDX tumor samples. 10X snRNA-seq data of the pHGG PDX sample combined into a pseudo-bulk compared to to bulk microarray data from a group of PDX samples based on correlation. The bulk microarray data of the same sample had the highest correlation to the 10X pseudo-bulk data (marked with an arrow). ( e ) t -distributed stochastic neighbour embedding (t-SNE) representation of combined 10X and C1 snRNA-seq datasets. ( f ) t-SNE representation of 10X PDX dataset. ( g ) Heatmap of pathways enriched among 10X PDX cell types. Colors represent confidence level –log10 (p-val). ( h ) Pseudotime trajectory analysis of 10X PDX cells. (i) Schematic representation of the identified tumor cell populations. See also Supplementary Fig. S2 and Supplementary Tables S2, S3, S4 and S5 online.

Article Snippet: Libraries from single nuclei were generated using either Chromium 10X Genomics , Fluidigm C1 or Drop-seq platforms according to the manufacturers’ instructions as described in Macosko et al and Bageritz et al (for Drop-seq).

Techniques: Comparison, Derivative Assay, Gene Expression, Microarray

Journal: Scientific Reports

Article Title: A simplified preparation method for single-nucleus RNA-sequencing using long-term frozen brain tumor tissues

doi: 10.1038/s41598-025-97053-9

Figure Lengend Snippet: SnRNA-seq of fresh frozen primary tumor tissues reveal distinct tumor and healthy cell populations. ( a ) Brightfield image showing intact isolated nuclei loaded to the 10X system (scale bar 10 μm). ( b ) t-SNE representation of pilocytic astrocytoma ICGC_PA56 snRNA-seq data. Two tumor clusters, oligodendrocyte precursor/oligodendrocyte -like (OPC/OC-like) and astrocyte-like (AC-like) tumor cells clearly separated from microglia and endothelial cells. ( c ) The most highly expressed marker genes show differential expression across assigned cell types. ( d ) OPC-like tumor cells and microglia form separate clusters detected from glioblastoma ICGC_GBM61 snRNA-seq data. 10X v3.1 snRNA-seq data of combined libraries of standard (approx. 300–1000 bp) and short (< 400 bp) cDNA fragments gives a more detailed clustering of the tumors, here ( e ) pilocytic astrocytoma ICGC_PA74 and ( f ) pleomorphic xanthoastrocytoma I007_024. ( g ) Some genes are detected only from the short library data, here ICGC_PA74 as example. See also Supplementary Fig. S3 and S4 and Supplementary Tables S2, S3, S4 and S5 online.

Article Snippet: Libraries from single nuclei were generated using either Chromium 10X Genomics , Fluidigm C1 or Drop-seq platforms according to the manufacturers’ instructions as described in Macosko et al and Bageritz et al (for Drop-seq).

Techniques: Isolation, Marker, Quantitative Proteomics

Journal: Scientific Reports

Article Title: A simplified preparation method for single-nucleus RNA-sequencing using long-term frozen brain tumor tissues

doi: 10.1038/s41598-025-97053-9

Figure Lengend Snippet: Copy number variation analysis supports tumor cell detection from 10 × snRNA- seq data. ( a ) Copy number variations (CNVs) of single nuclei from 10X snRNA-seq data of I007_024 analyzed by inferCNV. Non-malignant cells are used as control (upper heatmap). ( b ) A bulk CNV profile of the same tumor derived from Infinium HumanMethylation450 array analysis compared to pseudo-bulk extraction of CNV profiles from 10X data of I007_024 using mean values across the cells. See also Supplementary Fig. S5 and Supplementary Table S4 online.

Article Snippet: Libraries from single nuclei were generated using either Chromium 10X Genomics , Fluidigm C1 or Drop-seq platforms according to the manufacturers’ instructions as described in Macosko et al and Bageritz et al (for Drop-seq).

Techniques: Control, Derivative Assay, Extraction