P713: Estimating the prevalence of de novo monogenic disorders from gnomAD database

Ngā tūemi rite

• P713: Estimating the prevalence of de novo monogenic disorders from gnomAD database
  mā: Mutaz Amin, me ētahi atu.
  I whakaputaina: (2024-01-01)
• Improved allele frequencies in gnomAD through local ancestry inference
  mā: Pragati Kore, me ētahi atu.
  I whakaputaina: (2025-10-01)
• O43: Analysis of >800,000 diverse sequenced humans in gnomAD improves clinical interpretation and provides insight into gene function
  mā: Heidi Rehm, me ētahi atu.
  I whakaputaina: (2024-01-01)
• O11: An atlas of 1.2M structural variants across global populations in the Genome Aggregation Database (gnomAD)
  mā: Harrison Brand, me ētahi atu.
  I whakaputaina: (2024-01-01)
• Analysis of coding variants in the human FTO gene from the gnomAD database.
  mā: Mauro Lúcio Ferreira Souza Junior, me ētahi atu.
  I whakaputaina: (2022-01-01)