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stereo seq spatial transcriptomics platform  (Complete Genomics Inc)


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    Structured Review

    Complete Genomics Inc stereo seq spatial transcriptomics platform
    Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial <t>transcriptomics</t> with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.
    Stereo Seq Spatial Transcriptomics Platform, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 98/100, based on 34 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/stereo+seq+spatial+transcriptomics+platform/Stereo-seq+Transcriptomics+Set/pmc12955098-184-11-15
    Average 98 stars, based on 34 article reviews
    stereo seq spatial transcriptomics platform - by Bioz Stars, 2026-10
    98/100 stars

    Images

    1) Product Images from "Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription"

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

    Journal: eBioMedicine

    doi: 10.1016/j.ebiom.2026.106182

    Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.
    Figure Legend Snippet: Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.

    Techniques Used: Staining, Spatial Transcriptomics, Single Cell, Expressing, Activity Assay

    Related Articles

    Spatial Transcriptomics:

    Article Title: Single-cell Stereo-seq reveals regulatory mechanisms driving regeneration of injured proximal tubules during AKI.
    Article Snippet: .. Stereo-seq spatial transcriptomics data (BGI) were normalized using SCTransform in Seurat Spots with <1,000 total UMIs were filtered. ..

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription.
    Article Snippet: .. 6 www.thelancet.com Vol 125 ▪, 2026 Spatial transcriptomics data generation and analysis Formalin-fixed paraffin-embedded (FFPE) urothelial carcinoma tissue sections were profiled using the Stereo-seq spatial transcriptomics platform (MGI, China) according to the manufacturer’s protocols. ..

    Article Title: A Foundational Generative Model for Cross-platform Unified Enhancement of Spatial Transcriptomics
    Article Snippet: .. These include sequencing-based: Visium (probe-based and polyA-based) , Visium CytAssist , and VisiumHD (all Visium platforms are products of 10X Genomics), Spatial Transcriptomics (Spatial Transcriptomics AB), Stereo-seq (BGI), BMK S1000 (BMKGENE), and Open-ST , and image-based platforms: Xenium (10X Genomics) and CosMx (Nanostring). ..

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription
    Article Snippet: .. Formalin-fixed paraffin-embedded (FFPE) urothelial carcinoma tissue sections were profiled using the Stereo-seq spatial transcriptomics platform (MGI, China) according to the manufacturer's protocols. ..

    Formalin-fixed Paraffin-Embedded:

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription.
    Article Snippet: .. 6 www.thelancet.com Vol 125 ▪, 2026 Spatial transcriptomics data generation and analysis Formalin-fixed paraffin-embedded (FFPE) urothelial carcinoma tissue sections were profiled using the Stereo-seq spatial transcriptomics platform (MGI, China) according to the manufacturer’s protocols. ..

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription
    Article Snippet: .. Formalin-fixed paraffin-embedded (FFPE) urothelial carcinoma tissue sections were profiled using the Stereo-seq spatial transcriptomics platform (MGI, China) according to the manufacturer's protocols. ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: .. We used the STOmics Stereo-seq Transcriptomics Set for FFPE, which uses random primers to capture and sequence RNAs in situ . ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: across Countries with Varying Stomach Cancer Incidence Kie Kyon Huang1, Takeshi Hagihara1, Benedict Shi Xiang Lian1, Zhi Xuan Ong1, Shen Kiat Lim1, Roxanne Hui Heng Chong2, Supriya Srivastava2, Jason Xing Kang3, May Yin Lee4, Angie Lay-Keng Tan1, Minghui Lee1, Shamaine Wei Ting Ho4, Siti Aishah Binte Abdul Ghani1, Clara Shi Ya Ng1, Ruanyi Liang1, Lin Liu2, Su Ting Tay1, Xuewen Ong1, Feng Zhu2, Hui Chen5, Zhen Li5, Tiing Leong Ang6, Takuji Gotoda7,8, Robert J. Huang9, Christopher J.L.. Khor1,10, Hyun-Soo Kim11, Louis Ho Shing Lau12,13, Yi-Chia Lee14, Ayaka Takasu7,8, Ming Teh15, Mann Yie Thian16, Wai Leong Tam4,17,18,19, Xin Lu20, Sunny H. Wong3, Jimmy B.Y.. So21, Hyunsoo Chung22, Jonathan Lee2,23,24,25, Khay Guan Yeoh2,25, and Patrick Tan1,4,26,27,28; for the Singapore Gastric Cancer Consortium D ow nloaded from http://aacrjournals.org/cancerdiscovery/article-pdf/doi/10.1158/2159-8290.C D -25-0778/3726001/cd-25-0778.pdf by guest on 17 January 2026 AACRJournals.orgOF2 | CANCER DISCOVERY XXX 2026 intRoduction Gastric cancer is the fifth most common malignancy worldwide and the fourth leading cause of cancer death, accounting for 769,000 deaths globally in 2020 (1).

    Sequencing:

    Article Title: A Foundational Generative Model for Cross-platform Unified Enhancement of Spatial Transcriptomics
    Article Snippet: .. These include sequencing-based: Visium (probe-based and polyA-based) , Visium CytAssist , and VisiumHD (all Visium platforms are products of 10X Genomics), Spatial Transcriptomics (Spatial Transcriptomics AB), Stereo-seq (BGI), BMK S1000 (BMKGENE), and Open-ST , and image-based platforms: Xenium (10X Genomics) and CosMx (Nanostring). ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: .. We used the STOmics Stereo-seq Transcriptomics Set for FFPE, which uses random primers to capture and sequence RNAs in situ . ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: across Countries with Varying Stomach Cancer Incidence Kie Kyon Huang1, Takeshi Hagihara1, Benedict Shi Xiang Lian1, Zhi Xuan Ong1, Shen Kiat Lim1, Roxanne Hui Heng Chong2, Supriya Srivastava2, Jason Xing Kang3, May Yin Lee4, Angie Lay-Keng Tan1, Minghui Lee1, Shamaine Wei Ting Ho4, Siti Aishah Binte Abdul Ghani1, Clara Shi Ya Ng1, Ruanyi Liang1, Lin Liu2, Su Ting Tay1, Xuewen Ong1, Feng Zhu2, Hui Chen5, Zhen Li5, Tiing Leong Ang6, Takuji Gotoda7,8, Robert J. Huang9, Christopher J.L.. Khor1,10, Hyun-Soo Kim11, Louis Ho Shing Lau12,13, Yi-Chia Lee14, Ayaka Takasu7,8, Ming Teh15, Mann Yie Thian16, Wai Leong Tam4,17,18,19, Xin Lu20, Sunny H. Wong3, Jimmy B.Y.. So21, Hyunsoo Chung22, Jonathan Lee2,23,24,25, Khay Guan Yeoh2,25, and Patrick Tan1,4,26,27,28; for the Singapore Gastric Cancer Consortium D ow nloaded from http://aacrjournals.org/cancerdiscovery/article-pdf/doi/10.1158/2159-8290.C D -25-0778/3726001/cd-25-0778.pdf by guest on 17 January 2026 AACRJournals.orgOF2 | CANCER DISCOVERY XXX 2026 intRoduction Gastric cancer is the fifth most common malignancy worldwide and the fourth leading cause of cancer death, accounting for 769,000 deaths globally in 2020 (1).

    Transcriptomics:

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: .. We used the STOmics Stereo-seq Transcriptomics Set for FFPE, which uses random primers to capture and sequence RNAs in situ . ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: across Countries with Varying Stomach Cancer Incidence Kie Kyon Huang1, Takeshi Hagihara1, Benedict Shi Xiang Lian1, Zhi Xuan Ong1, Shen Kiat Lim1, Roxanne Hui Heng Chong2, Supriya Srivastava2, Jason Xing Kang3, May Yin Lee4, Angie Lay-Keng Tan1, Minghui Lee1, Shamaine Wei Ting Ho4, Siti Aishah Binte Abdul Ghani1, Clara Shi Ya Ng1, Ruanyi Liang1, Lin Liu2, Su Ting Tay1, Xuewen Ong1, Feng Zhu2, Hui Chen5, Zhen Li5, Tiing Leong Ang6, Takuji Gotoda7,8, Robert J. Huang9, Christopher J.L.. Khor1,10, Hyun-Soo Kim11, Louis Ho Shing Lau12,13, Yi-Chia Lee14, Ayaka Takasu7,8, Ming Teh15, Mann Yie Thian16, Wai Leong Tam4,17,18,19, Xin Lu20, Sunny H. Wong3, Jimmy B.Y.. So21, Hyunsoo Chung22, Jonathan Lee2,23,24,25, Khay Guan Yeoh2,25, and Patrick Tan1,4,26,27,28; for the Singapore Gastric Cancer Consortium D ow nloaded from http://aacrjournals.org/cancerdiscovery/article-pdf/doi/10.1158/2159-8290.C D -25-0778/3726001/cd-25-0778.pdf by guest on 17 January 2026 AACRJournals.orgOF2 | CANCER DISCOVERY XXX 2026 intRoduction Gastric cancer is the fifth most common malignancy worldwide and the fourth leading cause of cancer death, accounting for 769,000 deaths globally in 2020 (1).

    In Situ:

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: .. We used the STOmics Stereo-seq Transcriptomics Set for FFPE, which uses random primers to capture and sequence RNAs in situ . ..

    Article Title: Mutational Signatures and Clonal Hematopoiesis in Intestinal Metaplasia across Countries with Varying Stomach Cancer Incidence
    Article Snippet: across Countries with Varying Stomach Cancer Incidence Kie Kyon Huang1, Takeshi Hagihara1, Benedict Shi Xiang Lian1, Zhi Xuan Ong1, Shen Kiat Lim1, Roxanne Hui Heng Chong2, Supriya Srivastava2, Jason Xing Kang3, May Yin Lee4, Angie Lay-Keng Tan1, Minghui Lee1, Shamaine Wei Ting Ho4, Siti Aishah Binte Abdul Ghani1, Clara Shi Ya Ng1, Ruanyi Liang1, Lin Liu2, Su Ting Tay1, Xuewen Ong1, Feng Zhu2, Hui Chen5, Zhen Li5, Tiing Leong Ang6, Takuji Gotoda7,8, Robert J. Huang9, Christopher J.L.. Khor1,10, Hyun-Soo Kim11, Louis Ho Shing Lau12,13, Yi-Chia Lee14, Ayaka Takasu7,8, Ming Teh15, Mann Yie Thian16, Wai Leong Tam4,17,18,19, Xin Lu20, Sunny H. Wong3, Jimmy B.Y.. So21, Hyunsoo Chung22, Jonathan Lee2,23,24,25, Khay Guan Yeoh2,25, and Patrick Tan1,4,26,27,28; for the Singapore Gastric Cancer Consortium D ow nloaded from http://aacrjournals.org/cancerdiscovery/article-pdf/doi/10.1158/2159-8290.C D -25-0778/3726001/cd-25-0778.pdf by guest on 17 January 2026 AACRJournals.orgOF2 | CANCER DISCOVERY XXX 2026 intRoduction Gastric cancer is the fifth most common malignancy worldwide and the fourth leading cause of cancer death, accounting for 769,000 deaths globally in 2020 (1).

    other:

    Article Title: Single-cell spatiotemporal dissection of the human maternal-fetal interface.
    Article Snippet: Dissected tissues were sequentially washed to remove residual blood cells in DMEM/H-21 medium, supplemented with 12.5% FBS (Hyclone), 1% L-glutamine (Atlanta Biologicals), 1% penicillin/streptomycin and 0.1% gentamicin and cold 1× PBS (Gibco, Thermofisher).



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    Image Search Results


    Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.

    Journal: eBioMedicine

    Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

    doi: 10.1016/j.ebiom.2026.106182

    Figure Lengend Snippet: Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.

    Article Snippet: Formalin-fixed paraffin-embedded (FFPE) urothelial carcinoma tissue sections were profiled using the Stereo-seq spatial transcriptomics platform (MGI, China) according to the manufacturer's protocols.

    Techniques: Staining, Spatial Transcriptomics, Single Cell, Expressing, Activity Assay