single cell clustering data Search Results


86
10X Genomics hst data sets
Hst Data Sets, supplied by 10X Genomics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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90
Broad Institute Inc single cell sequencing portal
Single Cell Sequencing Portal, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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RStudio single-cell data matrix
Single Cell Data Matrix, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/single+cell+data+matrix/pmc08689354-679-2-10
Average 90 stars, based on 1 article reviews
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Broad Institute Inc single-cell transcriptomic data
Single Cell Transcriptomic Data, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Broad Institute Inc single cell umap data for linc01230
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Single Cell Umap Data For Linc01230, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/single+cell+umap+data+for+linc01230/pmc11334222-337-5-14
Average 90 stars, based on 1 article reviews
single cell umap data for linc01230 - by Bioz Stars, 2026-10
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90
Broad Institute Inc rna-seq data for breast cancers
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Rna Seq Data For Breast Cancers, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/single+cell+rna+sequencing+breast+cancer+atlas+data/pmc08405682-156-3-9
Average 90 stars, based on 1 article reviews
rna-seq data for breast cancers - by Bioz Stars, 2026-10
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90
Epigenomics ag binarized matrix of scatac or other single-cell epigenomics data
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Binarized Matrix Of Scatac Or Other Single Cell Epigenomics Data, supplied by Epigenomics ag, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/binarized+matrix+of+scatac+or+other+single+cell+epigenomics+data/pmc11613708-192-17-23
Average 90 stars, based on 1 article reviews
binarized matrix of scatac or other single-cell epigenomics data - by Bioz Stars, 2026-10
90/100 stars
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90
Allen Institute for Brain Science public mouse hippocampal single-cell data
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Public Mouse Hippocampal Single Cell Data, supplied by Allen Institute for Brain Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/public+mouse+hippocampal+single+cell+data/pmc09292385-167-0-9
Average 90 stars, based on 1 article reviews
public mouse hippocampal single-cell data - by Bioz Stars, 2026-10
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90
Allen Institute for Brain Science 10x v3 single-cell data
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
10x V3 Single Cell Data, supplied by Allen Institute for Brain Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/10x+v3+single+cell+data/pmc09882246-72-0-10
Average 90 stars, based on 1 article reviews
10x v3 single-cell data - by Bioz Stars, 2026-10
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90
WholeGenome LLC single-cell rna sequencing data
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Single Cell Rna Sequencing Data, supplied by WholeGenome LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/single+cell+rna+sequencing+data/pmc07363959__mmc3-80-13-25
Average 90 stars, based on 1 article reviews
single-cell rna sequencing data - by Bioz Stars, 2026-10
90/100 stars
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90
Omada Health Inc whole blood rnaseq dataset
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Whole Blood Rnaseq Dataset, supplied by Omada Health Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/single+cell+pbmc+data/pmc11238428__giae039_giga___d___23___00220_original_submission-194-25-5
Average 90 stars, based on 1 article reviews
whole blood rnaseq dataset - by Bioz Stars, 2026-10
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90
BioTuring Inc human ipf single-cell rna-seq data
(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN <t>(linc01230)</t> expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.
Human Ipf Single Cell Rna Seq Data, supplied by BioTuring Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/single+cell+clustering+data/human+ipf+single+cell+rna+seq+data/pmc09314350-371-2-11
Average 90 stars, based on 1 article reviews
human ipf single-cell rna-seq data - by Bioz Stars, 2026-10
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Image Search Results


(A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN (linc01230) expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.

Journal: Cell reports

Article Title: linc-ADAIN , a human adipose lincRNA, regulates adipogenesis by modulating KLF5 and IL-8 mRNA stability

doi: 10.1016/j.celrep.2024.114240

Figure Lengend Snippet: (A) Regulatory features at the linc-ADAIN locus, RNA-seq coverage (human adipocytes), transcription factor binding, and active histone modification markers. (B) Tissue expression of linc-ADAIN from GTEx (gene mean transcripts per million [TPM]). (C and D) Induction of linc-ADAIN by the PPARγ agonist rosiglitazone (10 μM) (C) and during adipocyte differentiation in vitro (D) ( N = 3 in triplicate). (E) Cellular fractionation of primary ASC adipocytes. qPCR of MALAT1, GAPDH, and linc-ADAIN of nuclear and cytoplasmic fractions. Data were normalized by averaging of loading controls GAPDH, β-ACTIN, MALAT1, U6, and HPRT and then subtracting the nucleus value and getting a fold change of gene expression compared to nucleus ( N = 3). (F) RNA scope assay showing the spatial expression of linc-ADAIN (red) and nuclei (DAPI/blue) in scramble and linc-ADAIN shRNA hTERT ASC adipocytes (scale bar, 20 μm). (G) UMAP (uniform manifold approximation and projection) projection of linc-ADAIN (linc01230) expression in single-cell RNA-seq of human subcutaneous WAT (Broad Institute ). Data are presented as the mean ± SEM.

Article Snippet: Single cell UMAP data for linc01230 was taken from the Single Cell Portal – Broad Institute ( https://singlecell.broadinstitute.org ) using single cell sequencing data from human white adipose tissue by Emont et al., 2022 .

Techniques: RNA Sequencing, Binding Assay, Modification, Expressing, In Vitro, Cell Fractionation, Gene Expression, RNAscope, shRNA