Connection

Co-Authors

This is a "connection" page, showing publications co-authored by FRITZ SEDLAZECK and Sairam Behera.
Connection Strength

5.534
  1. Comprehensive genome analysis and variant detection at scale using DRAGEN. Nat Biotechnol. 2024 Oct 25.
    View in: PubMed
    Score: 0.994
  2. Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk. BMC Med Genomics. 2024 10 24; 17(1):255.
    View in: PubMed
    Score: 0.994
  3. Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms. bioRxiv. 2024 Jan 06.
    View in: PubMed
    Score: 0.940
  4. Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk. bioRxiv. 2023 Apr 27.
    View in: PubMed
    Score: 0.896
  5. FixItFelix: improving genomic analysis by fixing reference errors. Genome Biol. 2023 02 21; 24(1):31.
    View in: PubMed
    Score: 0.885
  6. Publisher Correction: Detection of mosaic and population-level structural variants with Sniffles2. Nat Biotechnol. 2024 Oct; 42(10):1616.
    View in: PubMed
    Score: 0.247
  7. Detection of mosaic and population-level structural variants with Sniffles2. Nat Biotechnol. 2024 Oct; 42(10):1571-1580.
    View in: PubMed
    Score: 0.235
  8. Single-cell somatic copy number variants in brain using different amplification methods and reference genomes. Commun Biol. 2024 Oct 09; 7(1):1288.
    View in: PubMed
    Score: 0.062
  9. Single-cell somatic copy number variants in brain using different amplification methods and reference genomes. bioRxiv. 2023 Nov 21.
    View in: PubMed
    Score: 0.058
  10. Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation. Nat Methods. 2023 10; 20(10):1483-1492.
    View in: PubMed
    Score: 0.058
  11. Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes. Nat Methods. 2023 08; 20(8):1213-1221.
    View in: PubMed
    Score: 0.057
  12. Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation. bioRxiv. 2023 Apr 05.
    View in: PubMed
    Score: 0.056
  13. The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms. F1000Res. 2022; 11:530.
    View in: PubMed
    Score: 0.052
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.