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Connection

Bryan Howie to Genome, Human

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

0.347
  1. Haplotype estimation using sequencing reads. Am J Hum Genet. 2013 Oct 03; 93(4):687-96.
    View in: PubMed
    Score: 0.077
  2. The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome Res. 2013 May; 23(5):749-61.
    View in: PubMed
    Score: 0.074
  3. 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Eur J Hum Genet. 2012 Jul; 20(7):801-5.
    View in: PubMed
    Score: 0.069
  4. Comparing algorithms for genotype imputation. Am J Hum Genet. 2008 Oct; 83(4):535-9; author reply 539-40.
    View in: PubMed
    Score: 0.055
  5. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet. 2007 Jul; 39(7):906-13.
    View in: PubMed
    Score: 0.050
  6. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nat Commun. 2015 Sep 14; 6:8111.
    View in: PubMed
    Score: 0.022
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.