dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations ; volume:24 ; number:1 ; day:20 ; month:3 ; year:2023 ; pages:1-13 ; date:12.2023
BMC genomics ; 24, Heft 1 (20.3.2023), 1-13, 12.2023
- Creator
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Lv, Kangqi
Chen, Dayang
Xiong, Dan
Tang, Huamei
Ou, Tong
Kan, Lijuan
Zhang, Xiuming
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12864-023-09225-4
- URN
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urn:nbn:de:101:1-2023080821162802186224
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:51 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Lv, Kangqi
- Chen, Dayang
- Xiong, Dan
- Tang, Huamei
- Ou, Tong
- Kan, Lijuan
- Zhang, Xiuming
- SpringerLink (Online service)
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A novel scatterplot-based method to detect copy number variation (CNV)
ClassifyCNV: a tool for clinical annotation of copy-number variants
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples
CNV Radar: an improved method for somatic copy number alteration characterization in oncology
CNV-TV: A robust method to discover copy number variation from short sequencing reads
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
Copy number variation signature to predict human ancestry
Analyse von Copy Number Variationen (CNV) und Genfusionen in akuten myeloischen Leukämien mittels Nanopore-Sequenzierung
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication
Copy Number Variation (CNV) des Epidermalen Wachstumsfaktorrezeptors (EGFR) und das Metastasierungsverhalten von Brustkrebszellen im Mausmodell
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
A novel scatterplot-based method to detect copy number variation (CNV)
ClassifyCNV: a tool for clinical annotation of copy-number variants
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples
CNV Radar: an improved method for somatic copy number alteration characterization in oncology
CNV-TV: A robust method to discover copy number variation from short sequencing reads
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
Copy number variation signature to predict human ancestry
Analyse von Copy Number Variationen (CNV) und Genfusionen in akuten myeloischen Leukämien mittels Nanopore-Sequenzierung
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication