All Stories

  1. Cophenetic Spatial Topology Embedding reveals multiscale tissue architecture in spatial omics
  2. Targeted sequencing of mutations via RNA-templated gap filling of oligonucleotides for single-cell RNA-seq
  3. A dual genetic constraint underlies the conservation of early brains in vertebrates
  4. Spatially resolved microRNA expression in tissues: technologies, challenges, and opportunities
  5. A systematic implementation of padlock probing-based rolling circle amplification in an integrated microfluidic device for quantitative biomolecular analyses
  6. Spatial miRNomics: towards the integration of microRNAs in spatial biology
  7. Oligodendroglia vulnerability in the human dorsal striatum in Parkinson’s disease
  8. Data from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  9. Supplementary Figure S1 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  10. Supplementary Figure S2 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  11. Supplementary Figure S3 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  12. Supplementary Figure S4 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  13. Supplementary Figure S5 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  14. Supplementary Figure S6 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  15. Supplementary Figure S7 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  16. Supplementary Figure S8 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  17. Supplementary Table S1 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  18. Supplementary Table S2 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  19. Supplementary Table S3 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  20. Supplementary Table S4 from Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by <i>In Situ</i> Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  21. Spatial Transcriptome Mapping of the Desmoplastic Growth Pattern of Colorectal Liver Metastases by In Situ Sequencing Reveals a Biologically Relevant Zonation of the Desmoplastic Rim
  22. Interneuron diversity in the human dorsal striatum
  23. Spatial multimodal analysis of transcriptomes and metabolomes in tissues
  24. Tactile Tourism
  25. Spatial Multimodal Analysis of Transcriptomes and Metabolomes in Tissues
  26. De novo spatiotemporal modelling of cell-type signatures in the developmental human heart using graph convolutional neural networks
  27. Rolling Circle Amplification in Integrated Microsystems: An Uncut Gem toward Massively Multiplexed Pathogen Diagnostics and Genotyping
  28. Comprehensive in situ mapping of human cortical transcriptomic cell types
  29. Matisse: a MATLAB-based analysis toolbox for in situ sequencing expression maps
  30. Correction to ‘Hybridization-based in situ sequencing (HybISS) for spatially resolved transcriptomics in human and mouse brain tissue’
  31. Developmental landscape of human forebrain at a single-cell level unveils early waves of oligodendrogenesis
  32. De novo spatiotemporal modelling of cell-type signatures identifies novel cell populations in the developmental human heart
  33. Comprehensive in situ mapping of human cortical transcriptomic cell types
  34. Hybridization-based in situ sequencing (HybISS) for spatially resolved transcriptomics in human and mouse brain tissue
  35. Molecular architecture of the developing mouse brain
  36. Real‐time analysis of switchable nanocomposites of magnesium pyrophosphates and rolling circle amplification products
  37. SCRINSHOT, a spatial method for single-cell resolution mapping of cell states in tissue sections
  38. Probabilistic cell typing enables fine mapping of closely related cell types in situ
  39. Identification of spatial compartments in tissue from in situ sequencing data
  40. Padlock Probe Assay for Detection and Subtyping of Seasonal Influenza
  41. Smartphone-based clinical diagnostics: towards democratization of evidence-based health care
  42. Overcoming diagnostic issues in precision treatment of pancreatic cancer
  43. In Situ Detection and Quantification of AR-V7, AR-FL, PSA, andKRASPoint Mutations in Circulating Tumor Cells
  44. Simultaneous Single-Cell In Situ Analysis of Human Adenovirus Type 5 DNA and mRNA Expression Patterns in Lytic and Persistent Infection
  45. In Situ Single-Molecule RNA Genotyping Using Padlock Probes and Rolling Circle Amplification
  46. Multiplexed protein profiling by sequential affinity capture
  47. Rolling Circle Amplification with Padlock Probes for In Situ Detection of RNA Analytes
  48. A General Method for Rapid Determination of Antibiotic Susceptibility and Species in Bacterial Infections
  49. Circle-to-circle amplification on a digital microfluidic chip for amplified single molecule detection
  50. Molecular tools for companion diagnostics
  51. Point of care mutation detection
  52. Mosaic mutation detection: finding the rare ones
  53. Ligase-mediated Gene Detection
  54. PCR-generated padlock probes distinguish homologous chromosomes through quantitative fluorescence analysis
  55. Single‐Nucleotide Sequence Discrimination In Situ Using Padlock Probes
  56. Multiplex analysis of nucleic acid sequences by amplification of padlock probes on DNA arrays
  57. Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21
  58. Padlock probes: circularizing oligonucleotides for localized DNA detection
  59. Oligonucleotide Ligation Assay