Jan O. Korbel

European Molecular Biology Laboratory (EMBL), Heidelberg, Baden-Württemberg, Germany 
"Jan Korbel"
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Cross-listing: Computational Biology Tree

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Zhao X, Collins RL, Lee WP, et al. (2021) Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies. American Journal of Human Genetics
Ebert P, Audano PA, Zhu Q, et al. (2021) Haplotype-resolved diverse human genomes and integrated analysis of structural variation. Science (New York, N.Y.)
Roidos P, Sungalee S, Benfatto S, et al. (2020) A scalable CRISPR/Cas9-based fluorescent reporter assay to study DNA double-strand break repair choice. Nature Communications. 11: 4077
Drainas AP, Lambuta RA, Ivanova I, et al. (2020) Genome-wide Screens Implicate Loss of Cullin Ring Ligase 3 in Persistent Proliferation and Genome Instability in TP53-Deficient Cells. Cell Reports. 31: 107465
Calabrese C, Davidson NR, et al. (2020) Genomic basis for RNA alterations in cancer. Nature. 578: 129-136
Chaisson MJP, Sanders AD, Zhao X, et al. (2019) Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature Communications. 10: 1784
Gerhauser C, Favero F, Risch T, et al. (2018) Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell. 34: 996-1011.e8
Segura-Wang M, Onishi-Seebacher M, Stütz AM, et al. (2017) Systematic Identification of Determinants for Single Strand Annealing Mediated Deletion Formation in Saccharomyces cerevisiae. G3 (Bethesda, Md.)
Amin S, Awadalla P, Biankin A, et al. (2017) Abstract SY10-02: Pan-cancer study of recurrent and heterogeneous RNA aberrations and association with whole-genome variants Cancer Research. 77
Weischenfeldt J, Dubash T, Drainas AP, et al. (2016) Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking. Nature Genetics
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