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Sprod for de-noising spatially resolved transcriptomics data based on position and image information.
Wang, Yunguan; Song, Bing; Wang, Shidan; Chen, Mingyi; Xie, Yang; Xiao, Guanghua; Wang, Li; Wang, Tao.
Afiliação
  • Wang Y; Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Song B; Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Wang S; Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Chen M; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Xie Y; Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Xiao G; Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Wang L; Quantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Wang T; Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nat Methods ; 19(8): 950-958, 2022 08.
Article em En | MEDLINE | ID: mdl-35927477
Spatially resolved transcriptomics (SRT) provide gene expression close to, or even superior to, single-cell resolution while retaining the physical locations of sequencing and often also providing matched pathology images. However, SRT expression data suffer from high noise levels, due to the shallow coverage in each sequencing unit and the extra experimental steps required to preserve the locations of sequencing. Fortunately, such noise can be removed by leveraging information from the physical locations of sequencing, and the tissue organization reflected in corresponding pathology images. In this work, we developed Sprod, based on latent graph learning of matched location and imaging data, to impute accurate SRT gene expression. We validated Sprod comprehensively and demonstrated its advantages over previous methods for removing drop-outs in single-cell RNA-sequencing data. We showed that, after imputation by Sprod, differential expression analyses, pathway enrichment and cell-to-cell interaction inferences are more accurate. Overall, we envision de-noising by Sprod to become a key first step towards empowering SRT technologies for biomedical discoveries.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Transcriptoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos