Connection

KEN CHEN to Genome, Human

This is a "connection" page, showing publications KEN CHEN has written about Genome, Human.
Connection Strength

0.571
  1. CanDrA: cancer-specific driver missense mutation annotation with optimized features. PLoS One. 2013; 8(10):e77945.
    View in: PubMed
    Score: 0.064
  2. BreakTrans: uncovering the genomic architecture of gene fusions. Genome Biol. 2013 Aug 23; 14(8):R87.
    View in: PubMed
    Score: 0.063
  3. Whole-genome analysis informs breast cancer response to aromatase inhibition. Nature. 2012 Jun 10; 486(7403):353-60.
    View in: PubMed
    Score: 0.058
  4. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature. 2012 Jan 11; 481(7382):506-10.
    View in: PubMed
    Score: 0.057
  5. Massively parallel sequencing approaches for characterization of structural variation. Methods Mol Biol. 2012; 838:369-84.
    View in: PubMed
    Score: 0.057
  6. Genome remodelling in a basal-like breast cancer metastasis and xenograft. Nature. 2010 Apr 15; 464(7291):999-1005.
    View in: PubMed
    Score: 0.050
  7. BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nat Methods. 2009 Sep; 6(9):677-81.
    View in: PubMed
    Score: 0.048
  8. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature. 2008 Nov 06; 456(7218):66-72.
    View in: PubMed
    Score: 0.046
  9. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature. 2008 Oct 23; 455(7216):1061-8.
    View in: PubMed
    Score: 0.045
  10. Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med. 2013 05 30; 368(22):2059-74.
    View in: PubMed
    Score: 0.016
  11. Clonal architecture of secondary acute myeloid leukemia. N Engl J Med. 2012 Mar 22; 366(12):1090-8.
    View in: PubMed
    Score: 0.014
  12. SomaticSniper: identification of somatic point mutations in whole genome sequencing data. Bioinformatics. 2012 Feb 01; 28(3):311-7.
    View in: PubMed
    Score: 0.014
  13. Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. JAMA. 2011 Apr 20; 305(15):1568-76.
    View in: PubMed
    Score: 0.013
  14. Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. JAMA. 2011 Apr 20; 305(15):1577-84.
    View in: PubMed
    Score: 0.013
  15. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med. 2009 Sep 10; 361(11):1058-66.
    View in: PubMed
    Score: 0.012
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.