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Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting.

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Title: Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting.
Authors: Mazzonetto, Patricia C.1,2 (AUTHOR), Villela, Darine2 (AUTHOR), da Costa, Silvia Souza1 (AUTHOR), Krepischi, Ana C. V.1 (AUTHOR), Milanezi, Fernanda2 (AUTHOR), Migliavacca, Michele P.2 (AUTHOR), Pierry, Paulo M.2 (AUTHOR), Bonaldi, Adriano2 (AUTHOR), Almeida, Luiz Gustavo D.2 (AUTHOR), De Souza, Camila Alves2 (AUTHOR), Kroll, José Eduardo2 (AUTHOR), Paula, Marcelo G.2 (AUTHOR), Guarischi‐Sousa, Rodrigo2 (AUTHOR), Scapulatempo‐Neto, Cristovam2 (AUTHOR), Rosenberg, Carla1,2 (AUTHOR) carlarosenberg@ib.usp.br
Source: Annals of Human Genetics. Mar2024, Vol. 88 Issue 2, p113-125. 13p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Human+Genetics%22">Annals of Human Genetics</searchLink>. Mar2024, Vol. 88 Issue 2, p113-125. 13p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=175388431
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        Value: 10.1111/ahg.12532
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        Text: English
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              Text: Mar2024
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