RECOMB-CCB 2019 Schedule is avaliable here.
Keynote Talks
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Decoding epigenetic states of immune and cancer cellsTBAPathomics, Tumor Infiltrating Lymphocytes, Clinical Studies and Cancer Surveillance
Accepted Papers
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Deep Genomic Signature for early metastasis prediction in prostate cancer
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SCMarker: ab initio marker selection for single cell transcriptome profiling
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Uncovering and characterizing splice variants associated with survival in lung cancer patients
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Distance Measures for Tumor Evolutionary Trees
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Uncovering the subtype-specific temporal order of cancer pathway dysregulation
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SCIFIL: analysis of evolutionary history and clonal selection in cancer populations using single-cell sequencing data
Highlight Talks
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An Estrogen Regulated Feedback Loop Limits the Efficacy of Estrogen Receptor Targeted Breast Cancer Therapy
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Urea Cycle Dysregulation Generates Clinically Relevant Genomic and Biochemical Signatures
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Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling
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Inference of single-cell genotypes characterizes the genetic heterogeneity in pancreatic cancer precursor lesions
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Minimal functional driver gene heterogeneity among untreated metastases
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Integrated Transcriptomic-Genomic tool Texomer profiles cancer tissues
Late Breaking Research Talks
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Summarizing the Solution Space in Tumor Phylogeny Inference by Multiple Consensus Trees
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Chromatin-informed inference of transcriptional programs in gynecologic and basal breast cancers
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Single-cell phylogenetic inference with copy-number supported mutation losses
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Modeling Clinical and Molecular Covariates of Mutational Process Activity in Cancer
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Identifying Drug Sensitivity Subnetworks with NETPHLIX
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High-throughput binding prediction of Class I and Class II neoantigens with MHCnuggets
Accepted Posters
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Harnessing synthetic lethality to predict the response to cancer treatment
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Detection of Fraud in Large Omics Datasets
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CHASMplus reveals the scope of somatic missense mutations driving human cancers
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Atlas of Cancer Signaling Network: a resource of multi-scale biological maps to study disease mechanisms
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Comprehensive map of regulated cell death signalling network: a powerful analytical tool for studying diseases
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Systematic Discovery of the Functional Impact of Somatic Genome Alterations in Individual Tumors through Tumor-specific Causal Inference
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A Topology-Aware Edit Distance Measure For Cancer Evolutionary Trees
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Accurate quantification of copy-number aberrations and whole-genome duplications in multi-sample tumor sequencing data
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Effective clustering for single cell sequencing cancer data
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Ab initio Spillover Compensation in CyTOF Data
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Toward understanding mutagenesis in transcription factor binding sites
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Latent periodic process inference from single-cell RNA-seq data
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Methyl-sensitive transcription factor motifs in leukemia cell populations
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Tracing tumor cellular evolution through copy number alterations
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Contribution of synthetic lethality to cancer risk and onset time across human tissues
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Integrating (phospho)proteomics for improved identification of signal pathway abnormalities in cancer
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Network-based approaches elucidate differences within APOBEC and clock-like signatures in breast cancer
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Analysis of clustered mutations on highly mutated proteins in endometrial cancer
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Information Theoretic approaches to interrogate T-cell receptor diversity for cancer immunotherapy
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The Open Custom-Ranked Analysis of Variants Toolkit (OpenCRAVAT): A customizable annotation and prioritization pipeline for genes and variants
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ExploSig: Hypothesis-driven Exploration of Mutation Signature Etiology