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Sara Gosline

Publications

  • Knowledge-based classification of fine-grained immune cell types in single-cell RNA-Seq data with ImmClassifier
  • Pathway-based network modeling finds hidden genes in shRNA screen for regulators of acute lymphoblastic leukemia
  • Network modeling of kinase inhibitor polypharmacology reveals pathways targeted in chemical screens
  • A high-throughput molecular data resource for cutaneous neurofibromas
  • Systems approaches to cancer biology
  • Cutaneous neurofibromas in the genomics era: current understanding and open questions
  • The Superfund Research Program Analytics Portal: linking environmental chemical exposure to biological phenotypes
  • Refining protein subcellular localization.
  • SAMNet: A network-based approach to integrate multi-dimensional high throughput datasets
  • Antibody colocalization microarray: a scalable technology for multiplex protein analysis in complex samples.
  • Posttranscriptional regulation of per1 underlies the oncogenic function of IREα
  • Linking Proteomic and Transcriptional Data through the Interactome and Epigenome Reveals a Map of Oncogene-induced Signaling
  • SAMNetWeb: Identifying condition-specific networks linking signaling and transcription
  • Elucidating MicroRNA Regulatory Networks Using Transcriptional, Post-transcriptional, and Histone Modification Measurements
  • Supplemental Figures and Table from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Data from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Supplemental Figures and Table from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Data from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Proteome mapping of the human pancreatic islet microenvironment reveals endocrine-exocrine signaling sphere of influence
  • The AML microenvironment catalyzes a stepwise evolution to gilteritinib resistance.
  • Proteomic and phosphoproteomic measurements enhance ability to predict ex vivo drug response in AML.
  • Pharmacological and genomic profiling of neurofibromatosis type 1 plexiform neurofibroma-derived schwann cells
  • Decomprolute: A benchmarking platform designed for multiomics-based tumor deconvolution
  • Quantitative Proteomics Analysis of the Secretory Pathway
  • Intracellular eukaryotic parasites have a distinct unfolded protein response
  • Network-Based Interpretation of Diverse High-Throughput Datasets through the Omics Integrator Software Package
  • BayesDeBulk: A Flexible Bayesian Algorithm for the Deconvolution of Bulk Tumor Data
  • Probing the chemical-biological relationship space with the Drug Target Explorer
  • Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Integrative Analysis Identifies Candidate Tumor Microenvironment and Intracellular Signaling Pathways that Define Tumor Heterogeneity in NF1
  • leapR: An R Package for Multiomic Pathway Analysis
  • A field guide to cultivating computational biology
  • A rapid platform for 3D patient-derived cutaneous neurofibroma organoid establishment and screening
  • CDK4/6 inhibition enhances SHP2 inhibitor efficacy and is dependent upon restoration of RB function in malignant peripheral nerve sheath tumors
  • Ex vivo to in vivo model of malignant peripheral nerve sheath tumors for precision oncology
  • Mapping the proteogenomic landscape enables prediction of drug response in acute myeloid leukemia
  • Decomprolute is a benchmarking platform designed for multiomics-based tumor deconvolution
  • Supplemental Figures and Table from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Supplemental Figures and Table from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Data from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Data from Spatiotemporal Loss of NF1 in Schwann Cell Lineage Leads to Different Types of Cutaneous Neurofibroma Susceptible to Modification by the Hippo Pathway
  • Cutaneous neurofibromas in the genomics era: Current understanding and open questions
  • The evolution and multi-molecular properties of NF1 cutaneous neurofibromas originating from C-fiber sensory endings and terminal Schwann cells at normal sites of sensory terminations in the skin
  • Proteomics and Phosphoprotoemic Measurements Enhance Ability to Predict Ex Vivo Drug Response in AML
  • Integrated molecular and clinical analysis of low-grade gliomas in children with neurofibromatosis type 1 (NF1)
  • Engaging a community to enable disease-centric data sharing with the NF Data Portal
  • The AML Microenvironment Catalyzes a Step-Wise Evolution to Gilteritinib Resistance
  • Mass Spectrometry–Based Proteogenomics: New Therapeutic Opportunities for Precision Medicine
  • Proteogenomic data and resources for pan-cancer analysis
  • Utilizing proteomics and phosphoproteomics to predict ex vivo drug sensitivity across genetically diverse AML patients
  • Chromosome 8 gain is associated with high-grade transformation in MPNST
  • The TLK-ASF1 histone chaperone pathway plays a critical role in IL-1β–mediated AML progression
  • Mapping the Proteogenomic Landscape Enables Prediction of Drug Response in Acute Myeloid Leukemia
  • Pan-cancer analysis of post-translational modifications reveals shared patterns of protein regulation
  • Pan-cancer proteogenomics connects oncogenic drivers to functional states
  • A clinically and genomically annotated nerve sheath tumor biospecimen repository
  • Chromosome 8 gain is associated with high-grade transformation in MPNST
  • Knowledge-based classification of fine-grained immune cell types in single-cell RNA-Seq data
  • CDK4/6 inhibition enhances SHP2 inhibitor efficacy and is dependent upon RB function in malignant peripheral nerve sheath tumors
  • Integrative analysis identifies candidate tumor microenvironment and intracellular signaling pathways that define tumor heterogeneity in NF1
  • Integrative multi-omic cancer profiling reveals DNA methylation patterns associated with therapeutic vulnerability and cell-of-origin
  • A clinically and genomically annotated nerve sheath tumor biospecimen repository
  • Probing the chemical–biological relationship space with the Drug Target Explorer
  • Current and future directions in network biology
  • Deep learning integrates histopathology and proteogenomics at a pan-cancer level
  • Pan-cancer proteogenomics characterization of tumor immunity

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