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Connection

FRITZ SEDLAZECK to Neoplasms

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This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Neoplasms.
FRITZ SEDLAZECK
Connection Strength
0.633
Neoplasms
  1. Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T. Genome Res. 2025 Apr 14; 35(4):621-631.
    View in: PubMed
    Score: 0.326
  2. Unraveling the hidden complexity of cancer through long-read sequencing. Genome Res. 2025 Apr 14; 35(4):599-620.
    View in: PubMed
    Score: 0.082
  3. Germline structural variation globally impacts the cancer transcriptome including disease-relevant genes. Cell Rep Med. 2024 Mar 19; 5(3):101446.
    View in: PubMed
    Score: 0.075
  4. Searching thousands of genomes to classify somatic and novel structural variants using STIX. Nat Methods. 2022 04; 19(4):445-448.
    View in: PubMed
    Score: 0.066
  5. High resolution copy number inference in cancer using short-molecule nanopore sequencing. Nucleic Acids Res. 2021 12 02; 49(21):e124.
    View in: PubMed
    Score: 0.065
  6. Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapes. Cell Genom. 2024 Nov 13; 4(11):100674.
    View in: PubMed
    Score: 0.020
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.