Connection

CHRIS AMOS to Sequence Analysis, DNA

This is a "connection" page, showing publications CHRIS AMOS has written about Sequence Analysis, DNA.
Connection Strength

0.633
  1. Genomic sequencing in cancer. Cancer Lett. 2013 Nov 01; 340(2):161-70.
    View in: PubMed
    Score: 0.254
  2. Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models. Eur J Hum Genet. 2017 02; 25(3):350-359.
    View in: PubMed
    Score: 0.084
  3. Variants in melanocortin 1 receptor gene contribute to risk of melanoma--a direct sequencing analysis in a Texas population. Pigment Cell Melanoma Res. 2013 May; 26(3):422-5.
    View in: PubMed
    Score: 0.065
  4. Chipping away at the genetics of smoking behavior. Nat Genet. 2010 May; 42(5):366-8.
    View in: PubMed
    Score: 0.053
  5. A statistical learning method for simultaneous copy number estimation and subclone clustering with single-cell sequencing data. Genome Res. 2024 02 07; 34(1):85-93.
    View in: PubMed
    Score: 0.035
  6. Update on the State of the Science for Analytical Methods for Gene-Environment Interactions. Am J Epidemiol. 2017 Oct 01; 186(7):762-770.
    View in: PubMed
    Score: 0.022
  7. Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci Rep. 2015 Feb 05; 5:8278.
    View in: PubMed
    Score: 0.019
  8. A recurrent mutation in PARK2 is associated with familial lung cancer. Am J Hum Genet. 2015 Feb 05; 96(2):301-8.
    View in: PubMed
    Score: 0.018
  9. Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations. Clin Chem. 2014 Jul; 60(7):1004-11.
    View in: PubMed
    Score: 0.018
  10. A comprehensive assay for CFTR mutational analysis using next-generation sequencing. Clin Chem. 2013 Oct; 59(10):1481-8.
    View in: PubMed
    Score: 0.017
  11. Genetic variants in the vitamin D pathway and breast cancer disease-free survival. Carcinogenesis. 2013 Mar; 34(3):587-94.
    View in: PubMed
    Score: 0.016
  12. Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. J Natl Cancer Inst. 2008 Sep 17; 100(18):1326-30.
    View in: PubMed
    Score: 0.012
  13. TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. N Engl J Med. 2007 Sep 20; 357(12):1199-209.
    View in: PubMed
    Score: 0.011
  14. DNMT3b polymorphism and hereditary nonpolyposis colorectal cancer age of onset. Cancer Epidemiol Biomarkers Prev. 2006 May; 15(5):886-91.
    View in: PubMed
    Score: 0.010
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.