SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads ; volume:15 ; number:1 ; day:2 ; month:12 ; year:2024 ; pages:1-16 ; date:12.2024
Nature Communications ; 15, Heft 1 (2.12.2024), 1-16, 12.2024
- Creator
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41467-024-53087-7
- URN
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urn:nbn:de:101:1-2502162230313.037715396982
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:21 AM CEST
Data provider
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Associated
- Rajaby, Ramesh
- Sung, Wing-Kin
- SpringerLink (Online service)
Other Objects (12)
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PureCN: copy number calling and SNV classification using targeted short read sequencing
Local read haplotagging enables accurate long-read small variant calling
Towards pan-genome read alignment to improve variation calling
GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads
Empirical Bayes single nucleotide variant-calling for next-generation sequencing data
Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
Validation and assessment of variant calling pipelines for next-generation sequencing
Linkage disequilibrium based genotype calling from low-coverage shotgun sequencing reads
Base calling for high-throughput short-read sequencing: dynamic programming solutions
AdapterRemoval: easy cleaning of next-generation sequencing reads
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Classical solutions and their double copy in split signature
PureCN: copy number calling and SNV classification using targeted short read sequencing
Local read haplotagging enables accurate long-read small variant calling
Towards pan-genome read alignment to improve variation calling
GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads
Empirical Bayes single nucleotide variant-calling for next-generation sequencing data
Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
Validation and assessment of variant calling pipelines for next-generation sequencing
Linkage disequilibrium based genotype calling from low-coverage shotgun sequencing reads
Base calling for high-throughput short-read sequencing: dynamic programming solutions
AdapterRemoval: easy cleaning of next-generation sequencing reads
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing