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Connection

Tina Pesaran to Sequence Analysis, DNA

This is a "connection" page, showing publications Tina Pesaran has written about Sequence Analysis, DNA.
Connection Strength

0.943
  1. The Evolution of Constitutional Sequence Variant Interpretation. Clin Lab Med. 2020 06; 40(2):135-148.
    View in: PubMed
    Score: 0.679
  2. ClinGen and Genetic Testing. N Engl J Med. 2015 10; 373(14):1376-7.
    View in: PubMed
    Score: 0.123
  3. Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants. Hum Mutat. 2018 11; 39(11):1553-1568.
    View in: PubMed
    Score: 0.038
  4. Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion. Hum Mutat. 2018 11; 39(11):1517-1524.
    View in: PubMed
    Score: 0.038
  5. DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes. Genet Med. 2019 03; 21(3):683-693.
    View in: PubMed
    Score: 0.037
  6. Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genet Med. 2014 Nov; 16(11):830-7.
    View in: PubMed
    Score: 0.028
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.