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Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants.
Stoltze, Ulrik Kristoffer; Hagen, Christian Munch; van Overeem Hansen, Thomas; Byrjalsen, Anna; Gerdes, Anne-Marie; Yakimov, Victor; Rasmussen, Simon; Bækvad-Hansen, Marie; Hougaard, David Michael; Schmiegelow, Kjeld; Hjalgrim, Henrik; Wadt, Karin; Bybjerg-Grauholm, Jonas.
Afiliación
  • Stoltze UK; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark. ulrik.kristoffer.stoltze@regionh.dk.
  • Hagen CM; Department of Clinical Genetics, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark. ulrik.kristoffer.stoltze@regionh.dk.
  • van Overeem Hansen T; Department of Congenital Disorders, Statens Serum Institute, 2300, KBH S, Artillerivej 5, Denmark.
  • Byrjalsen A; Department of Clinical Genetics, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark.
  • Gerdes AM; Department of Clinical Medicine, Copenhagen University, Blegdamsvej 3B, 2200, KBH N, Denmark.
  • Yakimov V; Department of Clinical Genetics, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark.
  • Rasmussen S; Department of Clinical Genetics, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark.
  • Bækvad-Hansen M; Department of Congenital Disorders, Statens Serum Institute, 2300, KBH S, Artillerivej 5, Denmark.
  • Hougaard DM; Novo Nordisk Foundation Center for Protein Research, Copenhagen University, Blegdamsvej 3B, 2200, KBH N, Denmark.
  • Schmiegelow K; Department of Congenital Disorders, Statens Serum Institute, 2300, KBH S, Artillerivej 5, Denmark.
  • Hjalgrim H; Department of Congenital Disorders, Statens Serum Institute, 2300, KBH S, Artillerivej 5, Denmark.
  • Wadt K; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Blegdamsvej 9, 2100, KBH Ø, Denmark.
  • Bybjerg-Grauholm J; Department of Clinical Medicine, Copenhagen University, Blegdamsvej 3B, 2200, KBH N, Denmark.
Genome Med ; 15(1): 17, 2023 03 14.
Article en En | MEDLINE | ID: mdl-36918911
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Health_economic_evaluation / Prognostic_studies / Risk_factors_studies Límite: Child / Humans / Newborn Idioma: En Revista: Genome Med Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Health_economic_evaluation / Prognostic_studies / Risk_factors_studies Límite: Child / Humans / Newborn Idioma: En Revista: Genome Med Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca