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Genetics in Medicine Open
(Jan 2024)
P626: Clinical utility of structural variant calling using breakpoint analysis method for targeted NGS gene panels
Lotta Koskinen,
Margarita Andreevskaya,
Mikko Muona,
Tuuli Pietila,
Janica Djupsjöbacka,
Ville Kytölä,
Kati Kämpjärvi,
Samuel Myllykangas,
Pertteli Salmenperä,
Juha Koskenvuo,
Miko Valori
Affiliations
Lotta Koskinen
Blueprint Genetics, a Quest Diagnostics Company
Margarita Andreevskaya
Blueprint Genetics, a Quest Diagnostics Company
Mikko Muona
Blueprint Genetics, a Quest Diagnostics Company
Tuuli Pietila
Blueprint Genetics, a Quest Diagnostics Company
Janica Djupsjöbacka
Blueprint Genetics, a Quest Diagnostics Company
Ville Kytölä
Blueprint Genetics, a Quest Diagnostics Company
Kati Kämpjärvi
Blueprint Genetics, a Quest Diagnostics Company
Samuel Myllykangas
Blueprint Genetics, a Quest Diagnostics Company
Pertteli Salmenperä
Blueprint Genetics, a Quest Diagnostics Company
Juha Koskenvuo
Blueprint Genetics, a Quest Diagnostics Company
Miko Valori
Blueprint Genetics, a Quest Diagnostics Company
Journal volume & issue
Vol. 2
p. 101532
Abstract
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No abstracts available.
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