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

No abstracts available.

Published in Genetics in Medicine Open

ISSN: 2949-7744 (Online)
Publisher: Elsevier
Country of publisher: United States
LCC subjects: Science: Biology (General): Genetics; Medicine
Website: https://www.sciencedirect.com/journal/genetics-in-medicine-open

About the journal