ADAMOVÁ, Sabina, Kamila STRÁNSKÁ, Jan SVATOŇ, Michaela BOHÚNOVÁ, Eva ONDROUŠKOVÁ, Marie JAROŠOVÁ, Kristýna ZÁVACKÁ, Karolína ČERNOVSKÁ, Jana KOTAŠKOVÁ and Karla PLEVOVÁ. Application of long-read sequencing for detection of complex chromosomal rearrangements. In XXVIIth Biochemistry congress. 2023. ISBN 978-80-8240-048-2.
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Original name Application of long-read sequencing for detection of complex chromosomal rearrangements.
Authors ADAMOVÁ, Sabina, Kamila STRÁNSKÁ, Jan SVATOŇ, Michaela BOHÚNOVÁ, Eva ONDROUŠKOVÁ, Marie JAROŠOVÁ, Kristýna ZÁVACKÁ, Karolína ČERNOVSKÁ, Jana KOTAŠKOVÁ and Karla PLEVOVÁ.
Edition XXVIIth Biochemistry congress, 2023.
Other information
Original language English
Type of outcome Konferenční abstrakta
Country of publisher Slovakia
Confidentiality degree is not subject to a state or trade secret
WWW URL
Organization Středoevropský technologický institut – Repository – Repository
ISBN 978-80-8240-048-2
Keywords in English chromosomal abnormalities; In chronic lymphocytic leukemia; long-read sequencing
Links LX22NPO5102, research and development project. MUNI/A/1224/2022, interní kód Repo. NU21-08-00237, research and development project.
Changed by Changed by: RNDr. Daniel Jakubík, učo 139797. Changed: 25/3/2024 03:21.
Abstract
Complex karyotype (CK) typically involves various, often extensive numerical and structural chromosomal abnormalities. In chronic lymphocytic leukemia (CLL), it represents an established biomarker of adverse outcome. Common methods to detect CK include classical cytogenetics and genomic microarray; additional information may be obtained using next generation sequencing (NGS). However, all these approaches show low accuracy and sensitivity for detecting complex structural variants at the DNA sequence level. We aimed to explore the ability of long-read sequencing for the precise characterization of complex genomic variants in CLL patient samples.
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