All Stories

  1. Interpreting the functional impact of genetic variants: The need for context qualifiers
  2. Cancer treatments: Past, present, and future
  3. Improving transparency of computational tools for variant effect prediction
  4. Targeted Investigational Oncology Agents in the NCI-60: A Phenotypic Systems–based Resource
  5. Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
  6. TP53 isoform junction reads based analysis in malignant and normal contexts
  7. MutSpliceDB: A database of splice sites variants with RNA‐seq based evidence on effects on splicing
  8. Epigenome-wide DNA methylation analysis of small cell lung cancer cell lines suggests potential chemotherapy targets
  9. A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
  10. Standard operating procedure for curation and clinical interpretation of variants in cancer
  11. Early Detection is as Important as Imatinib in CML Treatment Success
  12. Are neuroendocrine negative small cell lung cancer and large cell neuroendocrine carcinoma with WT RB1 two faces of the same entity?
  13. Bioinformatics Tools and Resources for Cancer Immunotherapy Study
  14. Next-generation characterization of the Cancer Cell Line Encyclopedia
  15. Neuroendocrine negative SCLC is mostly RB1 WT and may be sensitive to CDK4/6 inhibition: Supplemental Tables
  16. Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community‐driven standards
  17. Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes
  18. ClinGen Cancer Somatic Working Group – standardizing and democratizing access to cancer molecular diagnostic data to drive translational research
  19. Detection of homozygous deletions in tumor-suppressor genes ranging from dozen to hundreds nucleotides in cancer models
  20. Small cell lung carcinoma cell line screen of etoposide/carboplatin plus a third agent
  21. Somatic cancer variant curation and harmonization through consensus minimum variant level data
  22. TP53Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data
  23. Small Cell Lung Cancer Screen of Oncology Drugs, Investigational Agents, and Gene and microRNA Expression
  24. Integrative modeling of multi-omics data to identify cancer drivers and infer patient-specific gene activity
  25. Pharmacogenomic agreement between two cancer cell line data sets
  26. Expression signature based on TP53 target genes doesn't predict response to TP53-MDM2 inhibitor in wild type TP53 tumors
  27. The identification and characterization of a STAT5 gene signature in hematologic malignancies
  28. Inhibiting Tankyrases Sensitizes KRAS-Mutant Cancer Cells to MEK Inhibitors via FGFR2 Feedback Signaling
  29. Integrative Radiogenomic Profiling of Squamous Cell Lung Cancer
  30. Tumor Suppressors Status in Cancer Cell Line Encyclopedia
  31. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
  32. Maintenance of adenomatous polyposis coli ( APC )-mutant colorectal cancer is dependent on Wnt/β-catenin signaling
  33. Genetic Mechanisms in Apc-Mediated Mammary Tumorigenesis
  34. Loss of Rb1 in the gastrointestinal tract of Apc 1638N mice promotes tumors of the cecum and proximal colon