Connection

BO PENG to Genome, Human

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

0.599
  1. Simulating sequences of the human genome with rare variants. Hum Hered. 2010; 70(4):287-91.
    View in: PubMed
    Score: 0.225
  2. WGSA: an annotation pipeline for human genome sequencing studies. J Med Genet. 2016 Feb; 53(2):111-2.
    View in: PubMed
    Score: 0.078
  3. Reproducible simulations of realistic samples for next-generation sequencing studies using Variant Simulation Tools. Genet Epidemiol. 2015 Jan; 39(1):45-52.
    View in: PubMed
    Score: 0.073
  4. Genetic Simulation Resources: a website for the registration and discovery of genetic data simulators. Bioinformatics. 2013 Apr 15; 29(8):1101-2.
    View in: PubMed
    Score: 0.065
  5. Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools. Bioinformatics. 2012 Feb 01; 28(3):421-2.
    View in: PubMed
    Score: 0.060
  6. Forward-time simulation of realistic samples for genome-wide association studies. BMC Bioinformatics. 2010 Sep 01; 11:442.
    View in: PubMed
    Score: 0.055
  7. Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases. J Bioinform Comput Biol. 2012 Apr; 10(2):1241008.
    View in: PubMed
    Score: 0.015
  8. Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinformatics. 2011 Aug 09; 12:331.
    View in: PubMed
    Score: 0.015
  9. A modified forward multiple regression in high-density genome-wide association studies for complex traits. Genet Epidemiol. 2009 Sep; 33(6):518-25.
    View in: PubMed
    Score: 0.013
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.