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  1. Article

    Open Access

    The methyltransferase domain of DNMT1 is an essential domain in acute myeloid leukemia independent of DNMT3A mutation

    Aberrant DNA methylation patterns are a prominent feature of cancer. Methylation of DNA is mediated by the DNA methyltransferase (DNMT) protein family, which regulates de novo (DNMT3A and DNMT3B) and maintenance ...

    Balpreet Bhogal, Barbara A. Weir, Ramona Crescenzo, Ann Marien in Communications Biology (2022)

  2. No Access

    Article

    Characterizing genomic alterations in cancer by complementary functional associations

    Complementary genomic features associated with pathway activation, gene dependency and drug sensitivity are uncovered using REVEALER.

    Jong Wook Kim, Olga B Botvinnik, Omar Abudayyeh, Chet Birger in Nature Biotechnology (2016)

  3. No Access

    Article

    High-throughput identification of genotype-specific cancer vulnerabilities in mixtures of barcoded tumor cell lines

    A method called PRISM rapidly identifies drug candidates that are effective against specific cancer cell lines.

    Channing Yu, Aristotle M Mannan, Griselda Metta Yvone in Nature Biotechnology (2016)

  4. No Access

    Article

    Absolute quantification of somatic DNA alterations in human cancer

    Tumors vary in their ratio of normal to cancerous cells and in their genomic copy number. Carter et al. describe an analytic method for inferring the purity and ploidy of a tumor sample, enabling longitudinal stu...

    Scott L Carter, Kristian Cibulskis, Elena Helman, Aaron McKenna in Nature Biotechnology (2012)

  5. No Access

    Article

    Towards patient-based cancer therapeutics

    Orienting cancer drug discovery to the patient requires relating the genetic features of tumors to acquired gene and pathway dependencies and identifying small-molecule therapeutics that target them.

    Stuart L Schreiber, Alykhan F Shamji, Paul A Clemons, Cindy Hon in Nature Biotechnology (2010)

  6. Article

    Open Access

    Major copy proportion analysis of tumor samples using SNP arrays

    Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the human genome and are useful as genomic markers. Oligonucleotide SNP microarrays have been developed for high-throughput geno...

    Cheng Li, Rameen Beroukhim, Barbara A Weir, Wendy Winckler in BMC Bioinformatics (2008)