single cell gene expression profiling Search Results


0.1x lysis buffer #cg000375  (10X Genomics)
90
10X Genomics 0.1x lysis buffer #cg000375
0.1x Lysis Buffer #Cg000375, supplied by 10X Genomics, 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+gene+expression+profiling/single+cell+multiome+atac+++gene+expression/pmc11252340-529-0-10
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0.1x lysis buffer #cg000375 - by Bioz Stars, 2026-11
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3’ single-cell gene expression libraries next gem v3.1  (10X Genomics)
90
10X Genomics 3’ single-cell gene expression libraries next gem v3.1
3’ Single Cell Gene Expression Libraries Next Gem V3.1, supplied by 10X Genomics, 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+gene+expression+profiling/3%E2%80%99+single+cell+gene+expression+libraries+next+gem+v3+1/med_rxiv__2024__07__24__24310960-191-12-21
Average 90 stars, based on 1 article reviews
3’ single-cell gene expression libraries next gem v3.1 - by Bioz Stars, 2026-11
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single cell gene expression platform  (10X Genomics)
90
10X Genomics single cell gene expression platform
(A) Ren1 is most highly expressed in JG populations and is absent, as expected, in Ren1 c KO populations. (B) Akr1b7, a surrogate JG marker, is expressed in renin-lineage populations with the highest <t>expression</t> in JG cells. SMC marker genes, including Acta2 (C), Smtn (D), Tagln (E), and Myh11 (F) are highly expressed in SMC cells and to a lesser degree in JG cells. (G) A <t>gene</t> signature of fibrosis is elevated in the fibrotic juxtaglomerular <t>cell</t> population (fbJG), leading to the assigned nomenclature. P value represents Welch’s T test.
Single Cell Gene Expression Platform, supplied by 10X Genomics, 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+gene+expression+profiling/single+cell+gene+expression/bio_rxiv__2025__07__09__663881-212-6-4
Average 90 stars, based on 1 article reviews
single cell gene expression platform - by Bioz Stars, 2026-11
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chromium single cell multiome atac + gene expression protocol  (Integragen sa)
90
Integragen sa chromium single cell multiome atac + gene expression protocol
(A) Ren1 is most highly expressed in JG populations and is absent, as expected, in Ren1 c KO populations. (B) Akr1b7, a surrogate JG marker, is expressed in renin-lineage populations with the highest <t>expression</t> in JG cells. SMC marker genes, including Acta2 (C), Smtn (D), Tagln (E), and Myh11 (F) are highly expressed in SMC cells and to a lesser degree in JG cells. (G) A <t>gene</t> signature of fibrosis is elevated in the fibrotic juxtaglomerular <t>cell</t> population (fbJG), leading to the assigned nomenclature. P value represents Welch’s T test.
Chromium Single Cell Multiome Atac + Gene Expression Protocol, supplied by Integragen sa, 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+gene+expression+profiling/chromium+single+cell+multiome+atac+++gene+expression+protocol/pm38311851-222-3-8
Average 90 stars, based on 1 article reviews
chromium single cell multiome atac + gene expression protocol - by Bioz Stars, 2026-11
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single cell gene expression data  (Human Protein Atlas)
90
Human Protein Atlas single cell gene expression data
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
Single Cell Gene Expression Data, supplied by Human Protein Atlas, 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+gene+expression+profiling/single+cell+gene+expression+data/pmc11345268-74-0-7
Average 90 stars, based on 1 article reviews
single cell gene expression data - by Bioz Stars, 2026-11
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single-cell gene expression profiling approaches  (Gaertner Scientific Corporation)
90
Gaertner Scientific Corporation single-cell gene expression profiling approaches
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
Single Cell Gene Expression Profiling Approaches, supplied by Gaertner Scientific Corporation, 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+gene+expression+profiling/single+cell+gene+expression+profiling+approaches/pmc07577590-787-31-18
Average 90 stars, based on 1 article reviews
single-cell gene expression profiling approaches - by Bioz Stars, 2026-11
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10x genomics protocol cg000338  (10X Genomics)
90
10X Genomics 10x genomics protocol cg000338
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
10x Genomics Protocol Cg000338, supplied by 10X Genomics, 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+gene+expression+profiling/chromium+next+gem+single+cell+multiome+atac+++gene+expression/ppr0738659-279-0-8
Average 90 stars, based on 1 article reviews
10x genomics protocol cg000338 - by Bioz Stars, 2026-11
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single cell multiome atac kit  (10X Genomics)
90
10X Genomics single cell multiome atac kit
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
Single Cell Multiome Atac Kit, supplied by 10X Genomics, 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+gene+expression+profiling/single+cell+multiome+atac+++gene+expression+kit/pmc10236001__pnas__2302019120__sapp-36-7-12
Average 90 stars, based on 1 article reviews
single cell multiome atac kit - by Bioz Stars, 2026-11
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3' v3 single cell expression kit  (10X Genomics)
90
10X Genomics 3' v3 single cell expression kit
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
3' V3 Single Cell Expression Kit, supplied by 10X Genomics, 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+gene+expression+profiling/single+cell+gene+expression+3%E2%80%99+v3+library+kit/pmc08924248-391-6-1
Average 90 stars, based on 1 article reviews
3' v3 single cell expression kit - by Bioz Stars, 2026-11
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5’ single cell gene expression, cell surface protein tag, tcr and bcr libraries  (10X Genomics)
90
10X Genomics 5’ single cell gene expression, cell surface protein tag, tcr and bcr libraries
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
5’ Single Cell Gene Expression, Cell Surface Protein Tag, Tcr And Bcr Libraries, supplied by 10X Genomics, 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+gene+expression+profiling/5%E2%80%99+single+cell+gene+expression++cell+surface+protein+tag++tcr+and+bcr+libraries/pmc10481789-571-0-0
Average 90 stars, based on 1 article reviews
5’ single cell gene expression, cell surface protein tag, tcr and bcr libraries - by Bioz Stars, 2026-11
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likelihood-ratio test for single cell gene expression  (McDavid Inc)
90
McDavid Inc likelihood-ratio test for single cell gene expression
Pathway and <t>cell</t> type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total <t>genes</t> represented. (B) Nasal epithelium specific genes with significantly differential <t>expression</t> in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by <t>single</t> cell transcriptome <t>data</t> as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).
Likelihood Ratio Test For Single Cell Gene Expression, supplied by McDavid 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+gene+expression+profiling/likelihood+ratio+test+for+single+cell+gene+expression/pmc06082168-668-17-25
Average 90 stars, based on 1 article reviews
likelihood-ratio test for single cell gene expression - by Bioz Stars, 2026-11
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spatial reconstruction of single-cell gene expression data  (Nature Biotechnology)
90
Nature Biotechnology spatial reconstruction of single-cell gene expression data
Distribution by top 10-record co-citations.
Spatial Reconstruction Of Single Cell Gene Expression Data, supplied by Nature Biotechnology, 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+gene+expression+profiling/spatial+reconstruction+of+single+cell+gene+expression+data/pmc08386406-46-11-16
Average 90 stars, based on 1 article reviews
spatial reconstruction of single-cell gene expression data - by Bioz Stars, 2026-11
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Image Search Results


(A) Ren1 is most highly expressed in JG populations and is absent, as expected, in Ren1 c KO populations. (B) Akr1b7, a surrogate JG marker, is expressed in renin-lineage populations with the highest expression in JG cells. SMC marker genes, including Acta2 (C), Smtn (D), Tagln (E), and Myh11 (F) are highly expressed in SMC cells and to a lesser degree in JG cells. (G) A gene signature of fibrosis is elevated in the fibrotic juxtaglomerular cell population (fbJG), leading to the assigned nomenclature. P value represents Welch’s T test.

Journal: bioRxiv

Article Title: Hypoxia-Induced Metabolic Reprogramming and Markings of Cell Fate in Concentric Arterial Hypertrophy

doi: 10.1101/2025.07.09.663881

Figure Lengend Snippet: (A) Ren1 is most highly expressed in JG populations and is absent, as expected, in Ren1 c KO populations. (B) Akr1b7, a surrogate JG marker, is expressed in renin-lineage populations with the highest expression in JG cells. SMC marker genes, including Acta2 (C), Smtn (D), Tagln (E), and Myh11 (F) are highly expressed in SMC cells and to a lesser degree in JG cells. (G) A gene signature of fibrosis is elevated in the fibrotic juxtaglomerular cell population (fbJG), leading to the assigned nomenclature. P value represents Welch’s T test.

Article Snippet: Fastq files from the 10X Genomics Single Cell Gene Expression platform were processed using the Cell Ranger pipeline (version: cellranger-7.2.0 ) and the refdata-gex-mm10-2020-A reference data.

Techniques: Marker, Expressing

Pathway and cell type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total genes represented. (B) Nasal epithelium specific genes with significantly differential expression in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by single cell transcriptome data as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).

Journal: Frontiers in Veterinary Science

Article Title: Host–microbe interactions in the nasal cavity of dogs with chronic idiopathic rhinitis

doi: 10.3389/fvets.2024.1385471

Figure Lengend Snippet: Pathway and cell type analysis for nasal transcriptome. (A) GSEA analysis results using Hallmarks and Biocarta pathways. Significant pathways organized by NES (normalized enrichment score) shown on x -axis from negative 3 to 3. FDR adjusted p -value shown in color scale, size of circles showing total genes represented. (B) Nasal epithelium specific genes with significantly differential expression in CR vs. HC comparison. Dot size shows normalized expression, x -axis shows Deseq fold change results (CR vs. HC). Color scale for FDR adjusted p -value (all <0.05). (C) Significant GSEA pathway associated with cilium, all downregulated in CR, normalized enrichment score (NES) shown on x -axis with total genes in pathway represented by dot size. (D) Cibersort was used to define cell types expressed in canine rhinitis or healthy samples represented in red and blue respectively. Normalized transcriptome count for 17,975 protein coding genes were used for analysis. Significance between disease vs. healthy groups was calculated using two way ANOVA with Bonferroni multiple comparisons test. X -axis shows cell types defined by single cell transcriptome data as described in methods, with dotted line on 10% total cell population. (C) Dot plot of nasal epithelium specific genes. Size shows noramalized expression value (average n = 11), FDR p -value shown in color (all <0.05).

Article Snippet: Single cell gene expression data from the Human Protein Atlas was used to identify olfactory and epithelial cell specific gene sets that were not expressed by immune cells.

Techniques: Quantitative Proteomics, Comparison, Expressing

Distribution by top 10-record co-citations.

Journal: Journal of Medical Internet Research

Article Title: Characterization of Global Research Trends and Prospects on Single-Cell Sequencing Technology: Bibliometric Analysis

doi: 10.2196/25789

Figure Lengend Snippet: Distribution by top 10-record co-citations.

Article Snippet: 10 , R Satija, 2015 , 605 , Spatial reconstruction of single-cell gene expression data , Nature Biotechnology.

Techniques: Sequencing, Marker, Gene Expression