software packages statview® v4.01 Search Results


docking calculations autodock v4.0.1  (AUTODOCK GmbH)
90
AUTODOCK GmbH docking calculations autodock v4.0.1
Docking Calculations Autodock V4.0.1, supplied by AUTODOCK GmbH, 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/software+packages+statview%C2%AE+v4%2E01/pmc05964670-120-19-18?v=AUTODOCK+GmbH
Average 90 stars, based on 1 article reviews
docking calculations autodock v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
knime v4.0.1  (KNIME GmbH)
90
KNIME GmbH knime v4.0.1
Knime V4.0.1, supplied by KNIME GmbH, 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/software+packages+statview%C2%AE+v4%2E01/pm34035124-66-19-18?v=KNIME+GmbH
Average 90 stars, based on 1 article reviews
knime v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
rstudio v4.0.1  (RStudio)
90
RStudio rstudio v4.0.1
Rstudio V4.0.1, 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/software+packages+statview%C2%AE+v4%2E01/pm37170127-249-14-13?v=RStudio
Average 90 stars, based on 1 article reviews
rstudio v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
seurat v4.0.1  (RStudio)
90
RStudio seurat v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Seurat V4.0.1, 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/software+packages+statview%C2%AE+v4%2E01/bio_rxiv__2021__07__04__451050-452-4-7?v=RStudio
Average 90 stars, based on 1 article reviews
seurat v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
remlogic v4.0.1  (Embla Systems)
90
Embla Systems remlogic v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Remlogic V4.0.1, supplied by Embla Systems, 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/software+packages+statview%C2%AE+v4%2E01/pmc12070486-141-24-26?v=Embla+Systems
Average 90 stars, based on 1 article reviews
remlogic v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
seqsphere + v4.0.1  (Ridom GmbH)
90
Ridom GmbH seqsphere + v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Seqsphere + V4.0.1, supplied by Ridom GmbH, 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/software+packages+statview%C2%AE+v4%2E01/pm30213965-272-10-10?v=Ridom+GmbH
Average 90 stars, based on 1 article reviews
seqsphere + v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
facsdiva v4.0.1  (Becton Dickinson)
90
Becton Dickinson facsdiva v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Facsdiva V4.0.1, supplied by Becton Dickinson, 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/software+packages+statview%C2%AE+v4%2E01/pm32393548-79-6-8?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
facsdiva v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
r v4.0.1  (RStudio)
90
RStudio r v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
R V4.0.1, 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/software+packages+statview%C2%AE+v4%2E01/pmc07822167-281-8-13?v=RStudio
Average 90 stars, based on 1 article reviews
r v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
program jmp v4.0.1  (SAS institute)
90
SAS institute program jmp v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Program Jmp V4.0.1, supplied by SAS institute, 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/software+packages+statview%C2%AE+v4%2E01/10__1017_slash_s0376892905002304-58-52-55?v=SAS+institute
Average 90 stars, based on 1 article reviews
program jmp v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
rigid-protein docking autodock v4.0.1  (AUTODOCK GmbH)
90
AUTODOCK GmbH rigid-protein docking autodock v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Rigid Protein Docking Autodock V4.0.1, supplied by AUTODOCK GmbH, 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/software+packages+statview%C2%AE+v4%2E01/pmc02908532-571-9-8?v=AUTODOCK+GmbH
Average 90 stars, based on 1 article reviews
rigid-protein docking autodock v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
qcleaner v4.0.1  (Amelieff Corporation)
90
Amelieff Corporation qcleaner v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Qcleaner V4.0.1, supplied by Amelieff 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/software+packages+statview%C2%AE+v4%2E01/pmc07971023-160-17-19?v=Amelieff+Corporation
Average 90 stars, based on 1 article reviews
qcleaner v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
climada v4.0.1  (ReCor Medical Inc)
90
ReCor Medical Inc climada v4.0.1
Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat <t>v4.0.1.</t> Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.
Climada V4.0.1, supplied by ReCor Medical 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/software+packages+statview%C2%AE+v4%2E01/pm38467707-179-5-10?v=ReCor+Medical+Inc
Average 90 stars, based on 1 article reviews
climada v4.0.1 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat v4.0.1. Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.

Journal: bioRxiv

Article Title: Fly Cell Atlas: a single-cell transcriptomic atlas of the adult fruit fly

doi: 10.1101/2021.07.04.451050

Figure Lengend Snippet: Integration of FCA snRNA-seq data and published scRNA-seq data of the ovary (A) FCA cells are highlighted in blue, and other cells are colored in gray. (B) Cells from the other three datasets are shown in orange, and FCA cells are displayed in gray. (C) Annotated FCA clusters as noted. Unannotated cells and cells from other datasets are in gray. (D) Polar cells identified in all datasets are highlighted and a magnified region of the UMAP plot containing polar cell clusters. (E) Unannotated FCA cells are labeled blue, all other cells are shown in gray. (F) Unannotated cells clustered independently. Presumptive cluster identities were determined by expression of marker genes as well as co-clustering with previously determined cell types. (G, H) Expression of sickie (sick) and Wnt4 genes labeling late stage terminal follicle cells indicated by arrows. (I, J) Confocal images of sick-GAL4 driving UAS-RFP showing expression in all late stage terminal follicle cells and of Wnt4-GAL4 driving UAS-RFP showing expression in low levels in posterior terminal follicle cells and in high levels in escort cells. Confocal images are maximum intensity projections. All plots are from UMAP. Three published adult ovarian scRNA-seq datasets are from ( ; ; ) . Datasets were integrated and batch corrected using Seurat v4.0.1. Scale bars in G and H depict average expression levels in log 2 (((UMI + 1)/total UMI)×10^4). Scale bar in I and J, 100 µm.

Article Snippet: Datasets were processed with Seurat v4.0.1 in RStudio Version 1.4.1103.

Techniques: Labeling, Expressing, Marker