Connection

BO PENG to High-Throughput Nucleotide Sequencing

This is a "connection" page, showing publications BO PENG has written about High-Throughput Nucleotide Sequencing.
  1. Empirical estimation of sequencing error rates using smoothing splines. BMC Bioinformatics. 2016 Apr 22; 17:177.
    View in: PubMed
    Score: 0.090
  2. 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: 0.082
  3. Variant association tools for quality control and analysis of large-scale sequence and genotyping array data. Am J Hum Genet. 2014 May 01; 94(5):770-83.
    View in: PubMed
    Score: 0.079
  4. 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: 0.067
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.