Validation and assessment of variant calling pipelines for next-generation sequencing
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1479-7364
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Validation and assessment of variant calling pipelines for next-generation sequencing ; volume:8 ; number:1 ; day:30 ; month:7 ; year:2014 ; pages:1-10 ; date:12.2014
Human genomics ; 8, Heft 1 (30.7.2014), 1-10, 12.2014
- Creator
-
Pirooznia, Mehdi
Kramer, Melissa
Parla, Jennifer
Goes, Fernando S.
Potash, James B.
McCombie, W Richard
Zandi, Peter P.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/1479-7364-8-14
- URN
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urn:nbn:de:101:1-2019102801411708548869
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:29 AM CEST
Data provider
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Associated
- Pirooznia, Mehdi
- Kramer, Melissa
- Parla, Jennifer
- Goes, Fernando S.
- Potash, James B.
- McCombie, W Richard
- Zandi, Peter P.
- SpringerLink (Online service)
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VDAP-GUI: a user-friendly pipeline for variant discovery and annotation of raw next-generation sequencing data
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Accuracy and efficiency of germline variant calling pipelines for human genome data
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Next-generation sequencing algorithms : from read mapping to variant detection
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iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data
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Empirical Bayes single nucleotide variant-calling for next-generation sequencing data
Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads
ToTem: a tool for variant calling pipeline optimization
VDAP-GUI: a user-friendly pipeline for variant discovery and annotation of raw next-generation sequencing data
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Accuracy and efficiency of germline variant calling pipelines for human genome data
ParticleCall: A particle filter for base calling in next-generation sequencing systems
Next-generation sequencing algorithms : from read mapping to variant detection
Next-generation sequencing algorithms : from read mapping to variant detection
iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data
Hereditary sensory and autonomic neuropathy : a next-generation sequencing analysis pipeline
Empirical Bayes single nucleotide variant-calling for next-generation sequencing data
Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
SurVIndel2: improving copy number variant calling from next-generation sequencing using hidden split reads
ToTem: a tool for variant calling pipeline optimization
VDAP-GUI: a user-friendly pipeline for variant discovery and annotation of raw next-generation sequencing data
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Accuracy and efficiency of germline variant calling pipelines for human genome data
ParticleCall: A particle filter for base calling in next-generation sequencing systems
Next-generation sequencing algorithms : from read mapping to variant detection
Next-generation sequencing algorithms : from read mapping to variant detection
iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data