Connection

Co-Authors

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

4.504
  1. Closing the gap: Solving complex medically relevant genes at scale. medRxiv. 2024 Mar 18.
    View in: PubMed
    Score: 0.994
  2. PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation. Genome Biol. 2021 09 14; 22(1):268.
    View in: PubMed
    Score: 0.835
  3. Publisher Correction: Detection of mosaic and population-level structural variants with Sniffles2. Nat Biotechnol. 2024 Jan 22.
    View in: PubMed
    Score: 0.246
  4. Detection of mosaic and population-level structural variants with Sniffles2. Nat Biotechnol. 2024 Jan 02.
    View in: PubMed
    Score: 0.245
  5. Genomic variant benchmark: if you cannot measure it, you cannot improve it. Genome Biol. 2023 10 05; 24(1):221.
    View in: PubMed
    Score: 0.241
  6. FixItFelix: improving genomic analysis by fixing reference errors. Genome Biol. 2023 02 21; 24(1):31.
    View in: PubMed
    Score: 0.231
  7. Fully resolved assembly of Cryptosporidium parvum. Gigascience. 2022 02 15; 11.
    View in: PubMed
    Score: 0.215
  8. Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 12 21; 9(12).
    View in: PubMed
    Score: 0.199
  9. Structural variant calling: the long and the short of it. Genome Biol. 2019 11 20; 20(1):246.
    View in: PubMed
    Score: 0.184
  10. Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structures. bioRxiv. 2023 Oct 03.
    View in: PubMed
    Score: 0.060
  11. Beyond the exome: What's next in diagnostic testing for Mendelian conditions. Am J Hum Genet. 2023 08 03; 110(8):1229-1248.
    View in: PubMed
    Score: 0.059
  12. Intratumoral Heterogeneity and Clonal Evolution Induced by HPV Integration. Cancer Discov. 2023 04 03; 13(4):910-927.
    View in: PubMed
    Score: 0.058
  13. Genome-Wide Analysis of Structural Variants in Parkinson Disease. Ann Neurol. 2023 05; 93(5):1012-1022.
    View in: PubMed
    Score: 0.057
  14. Beyond the exome: what's next in diagnostic testing for Mendelian conditions. ArXiv. 2023 Jan 18.
    View in: PubMed
    Score: 0.057
  15. Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism. Hum Mutat. 2022 12; 43(12):2033-2053.
    View in: PubMed
    Score: 0.056
  16. Construction of a new chromosome-scale, long-read reference genome assembly for the Syrian hamster, Mesocricetus auratus. Gigascience. 2022 05 28; 11.
    View in: PubMed
    Score: 0.055
  17. 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: 0.055
  18. Benchmarking challenging small variants with linked and long reads. Cell Genom. 2022 May; 2(5).
    View in: PubMed
    Score: 0.055
  19. Rescuing low frequency variants within intra-host viral populations directly from Oxford Nanopore sequencing data. Nat Commun. 2022 03 14; 13(1):1321.
    View in: PubMed
    Score: 0.054
  20. Curated variation benchmarks for challenging medically relevant autosomal genes. Nat Biotechnol. 2022 05; 40(5):672-680.
    View in: PubMed
    Score: 0.054
  21. Author Correction: Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nat Biotechnol. 2021 Nov; 39(11):1466.
    View in: PubMed
    Score: 0.053
  22. Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment. Gigascience. 2021 09 24; 10(9).
    View in: PubMed
    Score: 0.052
  23. Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nat Biotechnol. 2021 09; 39(9):1129-1140.
    View in: PubMed
    Score: 0.052
  24. Rescuing Low Frequency Variants within Intra-Host Viral Populations directly from Oxford Nanopore sequencing data. bioRxiv. 2021 Sep 06.
    View in: PubMed
    Score: 0.052
  25. 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: 0.050
  26. Chromosome-scale, haplotype-resolved assembly of human genomes. Nat Biotechnol. 2021 03; 39(3):309-312.
    View in: PubMed
    Score: 0.049
  27. Hidden genomic diversity of SARS-CoV-2: implications for qRT-PCR diagnostics and transmission. bioRxiv. 2020 Jul 02.
    View in: PubMed
    Score: 0.048
  28. Approaches to Whole Mitochondrial Genome Sequencing on the Oxford Nanopore MinION. Curr Protoc Hum Genet. 2019 12; 104(1):e94.
    View in: PubMed
    Score: 0.046
  29. A strategy for building and using a human reference pangenome. F1000Res. 2019; 8:1751.
    View in: PubMed
    Score: 0.046
  30. 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: 0.045
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.