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Connection

FRITZ SEDLAZECK to Genetic Variation

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This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Genetic Variation.
FRITZ SEDLAZECK
Connection Strength
1.643
Genetic Variation
  1. PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation. Genome Biol. 2021 09 14; 22(1):268.
    View in: PubMed
    Score: 0.480
  2. Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
    View in: PubMed
    Score: 0.152
  3. High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 Nov 20; 34(11):2061-2073.
    View in: PubMed
    Score: 0.149
  4. A complete reference genome improves analysis of human genetic variation. Science. 2022 04; 376(6588):eabl3533.
    View in: PubMed
    Score: 0.124
  5. SARS-CoV-2 genomic diversity and the implications for qRT-PCR diagnostics and transmission. Genome Res. 2021 04; 31(4):635-644.
    View in: PubMed
    Score: 0.115
  6. Discovery and population genomics of structural variation in a songbird genus. Nat Commun. 2020 07 07; 11(1):3403.
    View in: PubMed
    Score: 0.110
  7. A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet. 2019 11 07; 105(5):974-986.
    View in: PubMed
    Score: 0.105
  8. Ancestral Admixture Is the Main Determinant of Global Biodiversity in Fission Yeast. Mol Biol Evol. 2019 09 01; 36(9):1975-1989.
    View in: PubMed
    Score: 0.104
  9. Small variant benchmark from a complete assembly of X and Y chromosomes. Nat Commun. 2025 Jan 08; 16(1):497.
    View in: PubMed
    Score: 0.038
  10. StratoMod: predicting sequencing and variant calling errors with interpretable machine learning. Commun Biol. 2024 Oct 13; 7(1):1316.
    View in: PubMed
    Score: 0.037
  11. Unveiling novel genetic variants in 370 challenging medically relevant genes using the long read sequencing data of 41 samples from 19 global populations. Mol Genet Genomics. 2024 Jul 07; 299(1):65.
    View in: PubMed
    Score: 0.036
  12. The complete sequence of a human Y chromosome. Nature. 2023 Sep; 621(7978):344-354.
    View in: PubMed
    Score: 0.034
  13. Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals. PLoS One. 2021; 16(8):e0244468.
    View in: PubMed
    Score: 0.030
  14. A diploid assembly-based benchmark for variants in the major histocompatibility complex. Nat Commun. 2020 09 22; 11(1):4794.
    View in: PubMed
    Score: 0.028
  15. Targeted nanopore sequencing with Cas9-guided adapter ligation. Nat Biotechnol. 2020 04; 38(4):433-438.
    View in: PubMed
    Score: 0.027
  16. Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nat Biotechnol. 2019 10; 37(10):1155-1162.
    View in: PubMed
    Score: 0.026
  17. Duplication of a domestication locus neutralized a cryptic variant that caused a breeding barrier in tomato. Nat Plants. 2019 05; 5(5):471-479.
    View in: PubMed
    Score: 0.025
  18. The genomic basis of circadian and circalunar timing adaptations in a midge. Nature. 2016 12 01; 540(7631):69-73.
    View in: PubMed
    Score: 0.021
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.