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Connection

RICHARD GIBBS to Computational Biology

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This is a "connection" page, showing publications RICHARD GIBBS has written about Computational Biology.
RICHARD GIBBS
Connection Strength
1.084
Computational Biology
  1. Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Med. 2017 03 21; 9(1):26.
    View in: PubMed
    Score: 0.091
  2. Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort. Nucleic Acids Res. 2017 02 28; 45(4):1633-1648.
    View in: PubMed
    Score: 0.091
  3. Assessing structural variation in a personal genome-towards a human reference diploid genome. BMC Genomics. 2015 Apr 11; 16:286.
    View in: PubMed
    Score: 0.080
  4. Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies. Hum Mol Genet. 2015 Apr 15; 24(8):2125-37.
    View in: PubMed
    Score: 0.078
  5. Gene-specific function prediction for non-synonymous mutations in monogenic diabetes genes. PLoS One. 2014; 9(8):e104452.
    View in: PubMed
    Score: 0.076
  6. Comparative validation of the D. melanogaster modENCODE transcriptome annotation. Genome Res. 2014 Jul; 24(7):1209-23.
    View in: PubMed
    Score: 0.076
  7. Gene structure in the sea urchin Strongylocentrotus purpuratus based on transcriptome analysis. Genome Res. 2012 Oct; 22(10):2079-87.
    View in: PubMed
    Score: 0.066
  8. Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities. Genome Biol. 2011 Jul 25; 12(7):R68.
    View in: PubMed
    Score: 0.062
  9. SNPdetector: a software tool for sensitive and accurate SNP detection. PLoS Comput Biol. 2005 Oct; 1(5):e53.
    View in: PubMed
    Score: 0.042
  10. Dynamic building of a BAC clone tiling path for the Rat Genome Sequencing Project. Genome Res. 2004 Apr; 14(4):679-84.
    View in: PubMed
    Score: 0.037
  11. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. Am J Hum Genet. 2022 01 06; 109(1):81-96.
    View in: PubMed
    Score: 0.032
  12. Comparing vertebrate whole-genome shotgun reads to the human genome. Genome Res. 2001 Nov; 11(11):1807-16.
    View in: PubMed
    Score: 0.031
  13. muCNV: Genotyping Structural Variants for Population-level Sequencing. Bioinformatics. 2021 08 04; 37(14):2055?2057.
    View in: PubMed
    Score: 0.030
  14. Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgression. PLoS Biol. 2020 12; 18(12):e3000954.
    View in: PubMed
    Score: 0.030
  15. Shotgun sample sequence comparisons between mouse and human genomes. Nat Genet. 2000 May; 25(1):31-3.
    View in: PubMed
    Score: 0.028
  16. Hybrid de novo genome assembly and centromere characterization of the gray mouse lemur (Microcebus murinus). BMC Biol. 2017 Nov 16; 15(1):110.
    View in: PubMed
    Score: 0.024
  17. Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination. Genome Res. 1997 Mar; 7(3):268-80.
    View in: PubMed
    Score: 0.023
  18. DNAism: exploring genomic datasets on the web with Horizon Charts. BMC Bioinformatics. 2016 Jan 27; 17:49.
    View in: PubMed
    Score: 0.021
  19. The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes. BMC Genomics. 2015 Feb 28; 16:143.
    View in: PubMed
    Score: 0.020
  20. Mutational landscape of aggressive cutaneous squamous cell carcinoma. Clin Cancer Res. 2014 Dec 15; 20(24):6582-92.
    View in: PubMed
    Score: 0.019
  21. Whole-genome sequence-based analysis of high-density lipoprotein cholesterol. Nat Genet. 2013 Aug; 45(8):899-901.
    View in: PubMed
    Score: 0.018
  22. Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics. 2013 Oct; 102(4):270-7.
    View in: PubMed
    Score: 0.018
  23. A map of human genome variation from population-scale sequencing. Nature. 2010 Oct 28; 467(7319):1061-73.
    View in: PubMed
    Score: 0.015
  24. Metagenomic pyrosequencing and microbial identification. Clin Chem. 2009 May; 55(5):856-66.
    View in: PubMed
    Score: 0.013
  25. Novel microRNA candidates and miRNA-mRNA pairs in embryonic stem (ES) cells. PLoS One. 2008 Jul 02; 3(7):e2548.
    View in: PubMed
    Score: 0.012
  26. What everybody should know about the rat genome and its online resources. Nat Genet. 2008 May; 40(5):523-7.
    View in: PubMed
    Score: 0.012
  27. The complete genome of an individual by massively parallel DNA sequencing. Nature. 2008 Apr 17; 452(7189):872-6.
    View in: PubMed
    Score: 0.012
  28. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. 2004 Oct; 14(10B):2121-7.
    View in: PubMed
    Score: 0.010
  29. Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing. Genome Res. 2004 Apr; 14(4):665-71.
    View in: PubMed
    Score: 0.009
  30. The genome sequence of Drosophila melanogaster. Science. 2000 Mar 24; 287(5461):2185-95.
    View in: PubMed
    Score: 0.007
Connection Strength

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