O43: Analysis of >800,000 diverse sequenced humans in gnomAD improves clinical interpretation and provides insight into gene function

Samankaltaisia teoksia

• O43: Analysis of >800,000 diverse sequenced humans in gnomAD improves clinical interpretation and provides insight into gene function
  Tekijä: Heidi Rehm, et al.
  Julkaistu: (2024-01-01)
• P713: Estimating the prevalence of de novo monogenic disorders from gnomAD database
  Tekijä: Mutaz Amin, et al.
  Julkaistu: (2024-01-01)
• Improved allele frequencies in gnomAD through local ancestry inference
  Tekijä: Pragati Kore, et al.
  Julkaistu: (2025-10-01)
• P138: Evaluating the impact of gnomAD v4 on genetic prevalence estimates*
  Tekijä: Samantha Baxter, et al.
  Julkaistu: (2024-01-01)
• Analysis of coding variants in the human FTO gene from the gnomAD database.
  Tekijä: Mauro Lúcio Ferreira Souza Junior, et al.
  Julkaistu: (2022-01-01)