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  1. AU=Vandenbon Alexis
  2. AU="Alonso-Ventura, Vanesa"
  3. AU="Ganhewa, Aparna D"
  4. AU="Draggoo, V"
  5. AU="Natalia Skogberg"
  6. AU="Hiroaki Itoh" AU="Hiroaki Itoh"
  7. AU="Nicolette de Keizer"
  8. AU="Jamjoom, Dima"
  9. AU="Seeman, Tomas"
  10. AU="Popescu, S"
  11. AU="Kurtul, Irmak"
  12. AU="Christofferson, Scott"
  13. AU="Balghith, Mohammed A"
  14. AU="Banu, Qamar"
  15. AU="Giangregorio, Lora"
  16. AU="Stafiej, Patrycja"
  17. AU="Lau, Vincent W-H"
  18. AU="Francesca Storici"
  19. AU="Coulter-Mackie, Marion"
  20. AU="Mayank Goyal"
  21. AU="Lempke, Olga M"
  22. AU="Khan, Asad Majeed"
  23. AU=Ismail Mohd Iswadi
  24. AU="Jewel Park"
  25. AU="Hunter-Smith, David J"
  26. AU="Requião-Moura, Lúcio Roberto"
  27. AU=DesRochers Teresa M.
  28. AU="Kruschwitz, Sabine"
  29. AU=Sriwijiatalai Won
  30. AU="Bozzaro, Claudia"
  31. AU="Beckendorf, C"
  32. AU="Birge, N W"
  33. AU="Hoang, Oi Pui"
  34. AU="Saradha Baskaran"
  35. AU="Culotta, Lorenza"
  36. AU=Cleaver Ondine
  37. AU="Jordan A. Kreidberg"
  38. AU="Al-Marshoud, Majida"
  39. AU="David S Hui"
  40. AU="Manjappa, Shivaprasad"
  41. AU="Balkan, S"
  42. AU="Chen, Emma"
  43. AU="Delean, Ada"
  44. AU="Gurao, Ankita"
  45. AU="Lang, Zhen"
  46. AU="Mahnaz Mohammadpour"
  47. AU="Britta Grillitsch"
  48. AU=Hoeffner Ellen G
  49. AU="Al Harbi, Shmeylan"
  50. AU=Polevoda Bogdan
  51. AU="Raffaele Galiero"
  52. AU=Hruskova Z
  53. AU="Ayers, J"
  54. AU="Cohen, A D"
  55. AU="Brunetti, Gian Luca"
  56. AU=Andrade Daniel
  57. AU=Hay William W Jr

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  1. Artikel ; Online: Evaluation of critical data processing steps for reliable prediction of gene co-expression from large collections of RNA-seq data.

    Vandenbon, Alexis

    PloS one

    2022  Band 17, Heft 1, Seite(n) e0263344

    Abstract: Motivation: Gene co-expression analysis is an attractive tool for leveraging enormous amounts of public RNA-seq datasets for the prediction of gene functions and regulatory mechanisms. However, the optimal data processing steps for the accurate ... ...

    Abstract Motivation: Gene co-expression analysis is an attractive tool for leveraging enormous amounts of public RNA-seq datasets for the prediction of gene functions and regulatory mechanisms. However, the optimal data processing steps for the accurate prediction of gene co-expression from such large datasets remain unclear. Especially the importance of batch effect correction is understudied.
    Results: We processed RNA-seq data of 68 human and 76 mouse cell types and tissues using 50 different workflows into 7,200 genome-wide gene co-expression networks. We then conducted a systematic analysis of the factors that result in high-quality co-expression predictions, focusing on normalization, batch effect correction, and measure of correlation. We confirmed the key importance of high sample counts for high-quality predictions. However, choosing a suitable normalization approach and applying batch effect correction can further improve the quality of co-expression estimates, equivalent to a >80% and >40% increase in samples. In larger datasets, batch effect removal was equivalent to a more than doubling of the sample size. Finally, Pearson correlation appears more suitable than Spearman correlation, except for smaller datasets.
    Conclusion: A key point for accurate prediction of gene co-expression is the collection of many samples. However, paying attention to data normalization, batch effects, and the measure of correlation can significantly improve the quality of co-expression estimates.
    Mesh-Begriff(e) Animals ; Databases, Genetic ; Gene Expression Regulation ; Gene Ontology ; Gene Regulatory Networks ; Genome, Human ; Humans ; Linear Models ; Mice ; Models, Genetic ; RNA-Seq ; Reproducibility of Results ; Statistics, Nonparametric
    Sprache Englisch
    Erscheinungsdatum 2022-01-28
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0263344
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Evaluation of critical data processing steps for reliable prediction of gene co-expression from large collections of RNA-seq data.

    Alexis Vandenbon

    PLoS ONE, Vol 17, Iss 1, p e

    2022  Band 0263344

    Abstract: Motivation Gene co-expression analysis is an attractive tool for leveraging enormous amounts of public RNA-seq datasets for the prediction of gene functions and regulatory mechanisms. However, the optimal data processing steps for the accurate prediction ...

    Abstract Motivation Gene co-expression analysis is an attractive tool for leveraging enormous amounts of public RNA-seq datasets for the prediction of gene functions and regulatory mechanisms. However, the optimal data processing steps for the accurate prediction of gene co-expression from such large datasets remain unclear. Especially the importance of batch effect correction is understudied. Results We processed RNA-seq data of 68 human and 76 mouse cell types and tissues using 50 different workflows into 7,200 genome-wide gene co-expression networks. We then conducted a systematic analysis of the factors that result in high-quality co-expression predictions, focusing on normalization, batch effect correction, and measure of correlation. We confirmed the key importance of high sample counts for high-quality predictions. However, choosing a suitable normalization approach and applying batch effect correction can further improve the quality of co-expression estimates, equivalent to a >80% and >40% increase in samples. In larger datasets, batch effect removal was equivalent to a more than doubling of the sample size. Finally, Pearson correlation appears more suitable than Spearman correlation, except for smaller datasets. Conclusion A key point for accurate prediction of gene co-expression is the collection of many samples. However, paying attention to data normalization, batch effects, and the measure of correlation can significantly improve the quality of co-expression estimates.
    Schlagwörter Medicine ; R ; Science ; Q
    Thema/Rubrik (Code) 612
    Sprache Englisch
    Erscheinungsdatum 2022-01-01T00:00:00Z
    Verlag Public Library of Science (PLoS)
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  3. Artikel ; Online: A universal tool for predicting differentially active features in single-cell and spatial genomics data.

    Vandenbon, Alexis / Diez, Diego

    Scientific reports

    2023  Band 13, Heft 1, Seite(n) 11830

    Abstract: With the growing complexity of single-cell and spatial genomics data, there is an increasing importance of unbiased and efficient exploratory data analysis tools. One common exploratory data analysis step is the prediction of genes with different levels ... ...

    Abstract With the growing complexity of single-cell and spatial genomics data, there is an increasing importance of unbiased and efficient exploratory data analysis tools. One common exploratory data analysis step is the prediction of genes with different levels of activity in a subset of cells or locations inside a tissue. We previously developed singleCellHaystack, a method for predicting differentially expressed genes from single-cell transcriptome data, without relying on comparisons between clusters of cells. Here we present an update to singleCellHaystack, which is now a universally applicable method for predicting differentially active features: (1) singleCellHaystack now accepts continuous features that can be RNA or protein expression, chromatin accessibility or module scores from single-cell, spatial and even bulk genomics data, and (2) it can handle 1D trajectories, 2-3D spatial coordinates, as well as higher-dimensional latent spaces as input coordinates. Performance has been drastically improved, with up to ten times reduction in computational time and scalability to millions of cells, making singleCellHaystack a suitable tool for exploratory analysis of atlas level datasets. singleCellHaystack is available as packages in both R and Python.
    Mesh-Begriff(e) Software ; Gene Expression Profiling/methods ; Genomics/methods ; Transcriptome ; Data Analysis ; Single-Cell Analysis/methods
    Sprache Englisch
    Erscheinungsdatum 2023-07-22
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-38965-2
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Epigenetic characterization of housekeeping core promoters and their importance in tumor suppression.

    Loza, Martin / Vandenbon, Alexis / Nakai, Kenta

    Nucleic acids research

    2023  Band 52, Heft 3, Seite(n) 1107–1119

    Abstract: In this research, we elucidate the presence of around 11,000 housekeeping cis-regulatory elements (HK-CREs) and describe their main characteristics. Besides the trivial promoters of housekeeping genes, most HK-CREs reside in promoter regions and are ... ...

    Abstract In this research, we elucidate the presence of around 11,000 housekeeping cis-regulatory elements (HK-CREs) and describe their main characteristics. Besides the trivial promoters of housekeeping genes, most HK-CREs reside in promoter regions and are involved in a broader role beyond housekeeping gene regulation. HK-CREs are conserved regions rich in unmethylated CpG sites. Their distribution highly correlates with that of protein-coding genes, and they interact with many genes over long distances. We observed reduced activity of a subset of HK-CREs in diverse cancer subtypes due to aberrant methylation, particularly those located in chromosome 19 and associated with zinc finger genes. Further analysis of samples from 17 cancer subtypes showed a significantly increased survival probability of patients with higher expression of these genes, suggesting them as housekeeping tumor suppressor genes. Overall, our work unravels the presence of housekeeping CREs indispensable for the maintenance and stability of cells.
    Mesh-Begriff(e) Humans ; Promoter Regions, Genetic ; Regulatory Sequences, Nucleic Acid ; Gene Expression Regulation ; Neoplasms/genetics ; Epigenesis, Genetic
    Sprache Englisch
    Erscheinungsdatum 2023-12-12
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gkad1164
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Delamination of trophoblast-like syncytia from the amniotic ectodermal analogue in human primed embryonic stem cell-based differentiation model.

    Ohgushi, Masatoshi / Taniyama, Nobuko / Vandenbon, Alexis / Eiraku, Mototsugu

    Cell reports

    2022  Band 39, Heft 12, Seite(n) 110973

    Abstract: Human primed embryonic stem cells (ESCs) are known to be converted to cells with several trophoblast properties, but it has remained controversial whether this phenomenon represents the inherent differentiation competence of human primed ESCs to ... ...

    Abstract Human primed embryonic stem cells (ESCs) are known to be converted to cells with several trophoblast properties, but it has remained controversial whether this phenomenon represents the inherent differentiation competence of human primed ESCs to trophoblast lineages. In this study, we report that chemical blockage of ACTIVIN/NODAL and FGF signals is sufficient to steer human primed ESCs into GATA3-expressing cells that give rise to placental hormone-producing syncytia analogous to syncytiotrophoblasts of the post-implantation stage of the human embryo. Despite their cytological similarity to syncytiotrophoblasts, these syncytia arise from the non-trophoblastic differentiation trajectory that recapitulates amniogenesis. These results provide insights into the possible extraembryonic differentiation pathway that is unique in primate embryogenesis.
    Mesh-Begriff(e) Animals ; Cell Differentiation ; Embryonic Stem Cells/metabolism ; Female ; Giant Cells ; Humans ; Placenta ; Pregnancy ; Trophoblasts
    Sprache Englisch
    Erscheinungsdatum 2022-05-31
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2022.110973
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: A clustering-independent method for finding differentially expressed genes in single-cell transcriptome data.

    Vandenbon, Alexis / Diez, Diego

    Nature communications

    2020  Band 11, Heft 1, Seite(n) 4318

    Abstract: A common analysis of single-cell sequencing data includes clustering of cells and identifying differentially expressed genes (DEGs). How cell clusters are defined has important consequences for downstream analyses and the interpretation of results, but ... ...

    Abstract A common analysis of single-cell sequencing data includes clustering of cells and identifying differentially expressed genes (DEGs). How cell clusters are defined has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. To address this difficulty, we present singleCellHaystack, a method that enables the prediction of DEGs without relying on explicit clustering of cells. Our method uses Kullback-Leibler divergence to find genes that are expressed in subsets of cells that are non-randomly positioned in a multidimensional space. Comparisons with existing DEG prediction approaches on artificial datasets show that singleCellHaystack has higher accuracy. We illustrate the usage of singleCellHaystack through applications on 136 real transcriptome datasets and a spatial transcriptomics dataset. We demonstrate that our method is a fast and accurate approach for DEG prediction in single-cell data. singleCellHaystack is implemented as an R package and is available from CRAN and GitHub.
    Mesh-Begriff(e) Bone Marrow ; Cluster Analysis ; Computational Biology/methods ; Data Mining ; Gene Expression ; Gene Expression Profiling/methods ; Gene Regulatory Networks ; Single-Cell Analysis/methods ; Software ; Transcriptome
    Sprache Englisch
    Erscheinungsdatum 2020-08-28
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-020-17900-3
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: A clustering-independent method for finding differentially expressed genes in single-cell transcriptome data

    Alexis Vandenbon / Diego Diez

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Band 10

    Abstract: How cell clusters are defined in single-cell sequencing data has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. Here, the authors present a new approach that enables the prediction of ... ...

    Abstract How cell clusters are defined in single-cell sequencing data has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. Here, the authors present a new approach that enables the prediction of differentially expressed genes without relying on explicit clustering of cells.
    Schlagwörter Science ; Q
    Sprache Englisch
    Erscheinungsdatum 2020-08-01T00:00:00Z
    Verlag Nature Portfolio
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  8. Artikel ; Online: A clustering-independent method for finding differentially expressed genes in single-cell transcriptome data

    Alexis Vandenbon / Diego Diez

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Band 10

    Abstract: How cell clusters are defined in single-cell sequencing data has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. Here, the authors present a new approach that enables the prediction of ... ...

    Abstract How cell clusters are defined in single-cell sequencing data has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. Here, the authors present a new approach that enables the prediction of differentially expressed genes without relying on explicit clustering of cells.
    Schlagwörter Science ; Q
    Sprache Englisch
    Erscheinungsdatum 2020-08-01T00:00:00Z
    Verlag Nature Publishing Group
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  9. Artikel ; Online: Murine breast cancers disorganize the liver transcriptome in a zonated manner.

    Vandenbon, Alexis / Mizuno, Rin / Konishi, Riyo / Onishi, Masaya / Masuda, Kyoko / Kobayashi, Yuka / Kawamoto, Hiroshi / Suzuki, Ayako / He, Chenfeng / Nakamura, Yuki / Kawaguchi, Kosuke / Toi, Masakazu / Shimizu, Masahito / Tanaka, Yasuhito / Suzuki, Yutaka / Kawaoka, Shinpei

    Communications biology

    2023  Band 6, Heft 1, Seite(n) 97

    Abstract: The spatially organized gene expression program within the liver specifies hepatocyte functions according to their relative distances to the bloodstream (i.e., zonation), contributing to liver homeostasis. Despite the knowledge that solid cancers ... ...

    Abstract The spatially organized gene expression program within the liver specifies hepatocyte functions according to their relative distances to the bloodstream (i.e., zonation), contributing to liver homeostasis. Despite the knowledge that solid cancers remotely disrupt liver homeostasis, it remains unexplored whether solid cancers affect liver zonation. Here, using spatial transcriptomics, we thoroughly investigate the abundance and zonation of hepatic genes in cancer-bearing mice. We find that breast cancers affect liver zonation in various distinct manners depending on biological pathways. Aspartate metabolism and triglyceride catabolic processes retain relatively intact zonation patterns, but the zonation of xenobiotic catabolic process genes exhibits a strong disruption. The acute phase response is induced in zonated manners. Furthermore, we demonstrate that breast cancers activate innate immune cells in particular neutrophils in distinct zonated manners, rather than in a uniform fashion within the liver. Collectively, breast cancers disorganize hepatic transcriptomes in zonated manners, thereby disrupting zonated functions of the liver.
    Mesh-Begriff(e) Mice ; Animals ; Transcriptome ; Liver/metabolism ; Hepatocytes/metabolism ; Gene Expression Profiling ; Homeostasis ; Neoplasms/pathology
    Sprache Englisch
    Erscheinungsdatum 2023-01-24
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2399-3642
    ISSN (online) 2399-3642
    DOI 10.1038/s42003-023-04479-w
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Modeling the

    López, Yosvany / Vandenbon, Alexis / Nose, Akinao / Nakai, Kenta

    PeerJ

    2017  Band 5, Seite(n) e3389

    Abstract: Because transcription is the first step in the regulation of gene expression, understanding how transcription factors bind to their DNA binding motifs has become absolutely necessary. It has been shown that the promoters of genes with similar expression ... ...

    Abstract Because transcription is the first step in the regulation of gene expression, understanding how transcription factors bind to their DNA binding motifs has become absolutely necessary. It has been shown that the promoters of genes with similar expression profiles share common structural patterns. This paper presents an extensive study of the regulatory regions of genes expressed in 24 developmental stages of
    Sprache Englisch
    Erscheinungsdatum 2017-05-30
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2703241-3
    ISSN 2167-8359
    ISSN 2167-8359
    DOI 10.7717/peerj.3389
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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