How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia? | Zendy

Paola Bianchi | Zendy; Cristina Vercellati | Zendy; Elisa Fermo | Zendy

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How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?

Author(s) -

Paola Bianchi,

Cristina Vercellati,

Elisa Fermo

Publication year - 2020

Publication title -

annals of translational medicine

Language(s) - English

Resource type - Journals

eISSN - 2305-5847

pISSN - 2305-5839

DOI - 10.21037/atm.2020.02.151

Subject(s) - dna sequencing , computational biology , medicine , anemia , bioinformatics , biology , genetics , dna

UOC Ematologia, UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milano, Milan, Italy Correspondence to: Paola Bianchi, BSc, PhD. UOC Ematologia, UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milano, Via Francesco Sforza, 35, 20122 Milan, Italy. Email: paola.bianchi@policlinico.mi.it. Provenance and Peer Review: This article was commissioned by the Editorial Office, Annals of Translational Medicine. The article did not undergo external peer review. Comment on: Xue J, He Q, Xie X, et al. Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis. Ann Transl Med 2019;7:527.

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