CNV-seq, a new method to detect copy number variation using high-throughput sequencing
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2105
- 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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CNV-seq, a new method to detect copy number variation using high-throughput sequencing ; volume:10 ; number:1 ; day:06 ; month:3 ; year:2009 ; pages:1-9 ; date:12.2009
BMC bioinformatics ; 10, Heft 1 (06.3.2009), 1-9, 12.2009
- Creator
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Xie, Chao
- Contributor
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Tammi, Martti T.
SpringerLink (Online service)
- DOI
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10.1186/1471-2105-10-80
- URN
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urn:nbn:de:1111-201602178768
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:31 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Xie, Chao
- Tammi, Martti T.
- SpringerLink (Online service)
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SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data
Identification of chromosomal abnormalities in miscarriages by CNV-Seq
ClassifyCNV: a tool for clinical annotation of copy-number variants
Accurate and exact CNV identification from targeted high-throughput sequence data
dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
seqCNA: an R package for DNA copy number analysis in cancer using high-throughput sequencing
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
A novel scatterplot-based method to detect copy number variation (CNV)
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data
Identification of chromosomal abnormalities in miscarriages by CNV-Seq
ClassifyCNV: a tool for clinical annotation of copy-number variants
Accurate and exact CNV identification from targeted high-throughput sequence data
dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
seqCNA: an R package for DNA copy number analysis in cancer using high-throughput sequencing
MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples