Connection

FRITZ SEDLAZECK to Genome-Wide Association Study

This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Genome-Wide Association Study.
  1. Genome-Wide Analysis of Structural Variants in Parkinson Disease. Ann Neurol. 2023 05; 93(5):1012-1022.
    View in: PubMed
    Score: 0.125
  2. 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: 0.124
  3. 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: 0.119
  4. The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models. Cell. 2023 03 30; 186(7):1493-1511.e40.
    View in: PubMed
    Score: 0.032
  5. A multi-task convolutional deep neural network for variant calling in single molecule sequencing. Nat Commun. 2019 03 01; 10(1):998.
    View in: PubMed
    Score: 0.024
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.