All Stories

  1. BiocPkgTools: Toolkit for mining the Bioconductor package ecosystem
  2. BiocPkgTools: Toolkit for Mining the Bioconductor Package Ecosystem
  3. recount-brain: a curated repository of human brain RNA-seq datasets metadata
  4. restfulSE: A semantically rich interface for cloud-scale genomics with Bioconductor
  5. Orchestrating a community-developed computational workshop and accompanying training materials
  6. Resources for Interpreting Variants in Precision Genomic Oncology Applications
  7. Software For The Integration Of Multi-Omics Experiments In Bioconductor
  8. GenomicDataCommons: a Bioconductor Interface to the NCI Genomic Data Commons
  9. RARRES2 functions as a tumor suppressor by promoting β-catenin phosphorylation/degradation and inhibiting p38 phosphorylation in adrenocortical carcinoma
  10. Upregulation of IFN-Inducible and Damage-Response Pathways in Chronic Graft-versus-Host Disease
  11. On the Selective Packaging of Genomic RNA by HIV-1
  12. The Bioconductor channel in F1000Research
  13. Statistical Genomics
  14. The Bioconductor channel in F1000Research
  15. Integrated analysis of DNA methylation, immunohistochemistry and mRNA expression, data identifies a methylation expression index (MEI) robustly associated with survival of ER-positive breast cancer patients
  16. Super-enhancers delineate disease-associated regulatory nodes in T cells
  17. Orchestrating high-throughput genomic analysis with Bioconductor
  18. Antagonistic Cross-Regulation between Sox9 and Sox10 Controls an Anti-tumorigenic Program in Melanoma
  19. miR30a Inhibits LOX Expression and Anaplastic Thyroid Cancer Progression
  20. NCI-60 Whole Exome Sequencing and Pharmacological CellMiner Analyses
  21. Lineage of origin in rhabdomyosarcoma informs pharmacological response
  22. Genome-Wide Methylation Patterns in Papillary Thyroid Cancer Are Distinct Based on Histological Subtype and Tumor Genotype
  23. Downregulation of IGFBP2 is associated with resistance to IGF1R therapy in rhabdomyosarcoma
  24. Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33
  25. High prevalence of MAP2K1 mutations in variant and IGHV4-34–expressing hairy-cell leukemias
  26. A Polymorphism in IRF4 Affects Human Pigmentation through a Tyrosinase-Dependent MITF/TFAP2A Pathway
  27. Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer
  28. Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma
  29. The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology
  30. Whole Genome and Transcriptome Sequencing of a B3 Thymoma
  31. Harnessing genomics to identify environmental determinants of heritable disease
  32. RCircos: an R package for Circos 2D track plots
  33. Rb1 loss modifies but does not initiate alveolar rhabdomyosarcoma
  34. SRAdb: query and use public next-generation sequencing data from within R
  35. Chromothripsis and Focal Copy Number Alterations Determine Poor Outcome in Malignant Melanoma
  36. NCBI GEO: archive for functional genomics data sets—update
  37. Exclusion of the 750-kb genetically unstable region at Xq27 as a candidate locus for prostate malignancy in HPCX1-linked families
  38. Advanced Bone Formation in Mice with a Dominant-negative Mutation in the Thyroid Hormone Receptor β Gene due to Activation of Wnt/β-Catenin Protein Signaling
  39. In Vivo Role of Alternative Splicing and Serine Phosphorylation of the Microphthalmia-Associated Transcription Factor
  40. Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma
  41. Genome-Wide Methylation Profiling in Archival Formalin-Fixed Paraffin-Embedded Tissue Samples
  42. Genome-wide depletion of replication initiation events in highly transcribed regions
  43. CHEK2 genomic and proteomic analyses reveal genetic inactivation or endogenous activation across the 60 cell lines of the US National Cancer Institute
  44. A Methyl-Deviator Epigenotype of Estrogen Receptor–Positive Breast Carcinoma Is Associated with Malignant Biology
  45. Identification of an Inhibitor of the EWS-FLI1 Oncogenic Transcription Factor by High-Throughput Screening
  46. Preferential Localization of Human Origins of DNA Replication at the 5′-Ends of Expressed Genes and at Evolutionarily Conserved DNA Sequences
  47. Exome sequencing identifies GRIN2A as frequently mutated in melanoma
  48. Evidence for an Unanticipated Relationship between Undifferentiated Pleomorphic Sarcoma and Embryonal Rhabdomyosarcoma
  49. Interferon-γ links ultraviolet radiation to melanomagenesis in mice
  50. Archival Fine-Needle Aspiration Cytopathology (FNAC) Samples
  51. High frequencies of leukemia stem cells in poor-outcome childhood precursor-B acute lymphoblastic leukemias
  52. Epigenomic alterations and gene expression profiles in respiratory epithelia exposed to cigarette smoke condensate
  53. Assessment of Automated Image Analysis of Breast Cancer Tissue Microarrays for Epidemiologic Studies
  54. Vorinostat Inhibits Brain Metastatic Colonization in a Model of Triple-Negative Breast Cancer and Induces DNA Double-Strand Breaks
  55. Analyses of Resected Human Brain Metastases of Breast Cancer Reveal the Association between Up-Regulation of Hexokinase 2 and Poor Prognosis
  56. A Molecular Function Map of Ewing's Sarcoma
  57. Kinetic Complexity of the Global Response to Glucocorticoid Receptor Action
  58. Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma
  59. Large-Scale Profiling of Archival Lymph Nodes Reveals Pervasive Remodeling of the Follicular Lymphoma Methylome
  60. Canine tumor cross-species genomics uncovers targets linked to osteosarcoma progression
  61. Molecular Grading of Ductal Carcinoma In situ of the Breast
  62. GEOmetadb: powerful alternative search engine for the Gene Expression Omnibus
  63. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
  64. Interaction of the Glucocorticoid Receptor with the Chromatin Landscape
  65. TRAIL induces apoptosis in triple-negative breast cancer cells with a mesenchymal phenotype
  66. Suppressor role of activating transcription factor 2 (ATF2) in skin cancer
  67. High-Resolution Mapping and Characterization of Open Chromatin across the Genome
  68. Constitutive Fms-like tyrosine kinase 3 activation results in specific changes in gene expression in myeloid leukaemic cells
  69. Detection of Novel Amplicons in Prostate Cancer by Comprehensive Genomic Profiling of Prostate Cancer Cell Lines Using Oligonucleotide-Based ArrayCGH
  70. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
  71. A Single IGF1 Allele Is a Major Determinant of Small Size in Dogs
  72. Modeling Synovial Sarcoma: Timing Is Everything
  73. DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays
  74. Ewing's sarcoma: General insights from a rare model
  75. Genome-Wide Analysis of Menin Binding Provides Insights into MEN1 Tumorigenesis
  76. [14] Statistics for ChIP‐chip and DNase Hypersensitivity Experiments on NimbleGen Arrays
  77. Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS)
  78. Gene Expression Profiling of Human Sarcomas: Insights into Sarcoma Biology
  79. BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis
  80. Database of mRNA gene expression profiles of multiple human organs
  81. Impact of overlapping recruitment on linkage analysis of complex disorders: Simulation studies
  82. Linkage and Association between Inflammatory Bowel Disease and a Locus on Chromosome 12
  83. Comparison of Nonparametric Statistics for Detection of Linkage in Nuclear Families: Single-Marker Evaluation
  84. Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10
  85. Analysis of bipolar disorder using affected relatives
  86. Analysis of bipolar disorder using affected relatives
  87. Analysis of complex oligogenic disease
  88. Analysis of complex oligogenic disease
  89. Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13