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This is a "connection" page, showing publications co-authored by ERIC BOERWINKLE and FRITZ SEDLAZECK.
ERIC BOERWINKLE
Connection Strength
1.289
FRITZ SEDLAZECK
  1. Structural variation across 138,134 samples in the TOPMed consortium. Res Sq. 2023 Feb 03.
    View in: PubMed
    Score: 0.230
  2. Structural variation across 138,134 samples in the TOPMed consortium. bioRxiv. 2023 Jan 25.
    View in: PubMed
    Score: 0.230
  3. xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments. Gigascience. 2022 Dec 28; 12.
    View in: PubMed
    Score: 0.228
  4. muCNV: Genotyping Structural Variants for Population-level Sequencing. Bioinformatics. 2021 Mar 24.
    View in: PubMed
    Score: 0.202
  5. Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 12 21; 9(12).
    View in: PubMed
    Score: 0.199
  6. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. Nat Commun. 2022 12 08; 13(1):7592.
    View in: PubMed
    Score: 0.057
  7. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data. Am J Hum Genet. 2022 06 02; 109(6):1175-1181.
    View in: PubMed
    Score: 0.055
  8. A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet. 2019 11 07; 105(5):974-986.
    View in: PubMed
    Score: 0.046
  9. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel. Genet Med. 2019 09; 21(9):2135-2144.
    View in: PubMed
    Score: 0.044
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.