Read count-based method for high-throughput allelic genotyping of transposable elements and structural variants
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2164
- 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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Read count-based method for high-throughput allelic genotyping of transposable elements and structural variants ; volume:16 ; number:1 ; day:8 ; month:7 ; year:2015 ; pages:1-16 ; date:12.2015
BMC genomics ; 16, Heft 1 (8.7.2015), 1-16, 12.2015
- Creator
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Kuhn, Alexandre
Ong, Yao Min
Quake, Stephen R.
Burkholder, William F.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12864-015-1700-4
- URN
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urn:nbn:de:101:1-2021081507432790654872
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:58 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kuhn, Alexandre
- Ong, Yao Min
- Quake, Stephen R.
- Burkholder, William F.
- SpringerLink (Online service)
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Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication
Transposable elements
Copy number variation detection using next generation sequencing read counts
Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences
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DNA read count calibration for single-molecule, long-read sequencing
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
mmquant: how to count multi-mapping reads?
Evaluation of read count based RNAseq analysis methods
Allelic diversification after transposable element exaptation promoted gsdf as the master sex determining gene of sablefish
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
Comparison of Plasmodium falciparum allelic frequency distribution in different endemic settings by high-resolution genotyping
Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication
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Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences