ngs_backbone: a pipeline for read cleaning, mapping and SNP calling using Next Generation Sequence
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2164
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
ngs_backbone: a pipeline for read cleaning, mapping and SNP calling using Next Generation Sequence ; volume:12 ; number:1 ; day:2 ; month:6 ; year:2011 ; pages:1-8 ; date:12.2011
BMC genomics ; 12, Heft 1 (2.6.2011), 1-8, 12.2011
- Creator
-
Blanca, Jose M.
- Contributor
-
Pascual, Laura
Ziarsolo, Peio
Nuez, Fernando
Cañizares, Joaquin
SpringerLink (Online service)
- DOI
-
10.1186/1471-2164-12-285
- URN
-
urn:nbn:de:1111-2016072828306
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
2025-08-14T10:50:49+0200
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
- Blanca, Jose M.
- Pascual, Laura
- Ziarsolo, Peio
- Nuez, Fernando
- Cañizares, Joaquin
- SpringerLink (Online service)
Other Objects (12)
SNP calling by sequencing pooled samples
Understanding the Basics of NGS: From Mechanism to Variant Calling
Bis-SNP: Combined DNA methylation and SNP calling for Bisulfite-seq data
Comparing a few SNP calling algorithms using low-coverage sequencing data
A short tutorial in analyzing NGS data of cancer genomes for somatic mutation calling
A secure SNP panel scheme using homomorphically encrypted K-mers without SNP calling on the user side
NGS
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Duet: SNP-assisted structural variant calling and phasing using Oxford nanopore sequencing
Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data
SNiPer: Improved SNP genotype calling for Affymetrix 10K GeneChip microarray data
SNP calling by sequencing pooled samples
Understanding the Basics of NGS: From Mechanism to Variant Calling
Bis-SNP: Combined DNA methylation and SNP calling for Bisulfite-seq data
Comparing a few SNP calling algorithms using low-coverage sequencing data
A short tutorial in analyzing NGS data of cancer genomes for somatic mutation calling
A secure SNP panel scheme using homomorphically encrypted K-mers without SNP calling on the user side
NGS
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Duet: SNP-assisted structural variant calling and phasing using Oxford nanopore sequencing
Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data
SNiPer: Improved SNP genotype calling for Affymetrix 10K GeneChip microarray data
SNP calling by sequencing pooled samples
Understanding the Basics of NGS: From Mechanism to Variant Calling
Bis-SNP: Combined DNA methylation and SNP calling for Bisulfite-seq data
Comparing a few SNP calling algorithms using low-coverage sequencing data
A short tutorial in analyzing NGS data of cancer genomes for somatic mutation calling
A secure SNP panel scheme using homomorphically encrypted K-mers without SNP calling on the user side
NGS
Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing
Duet: SNP-assisted structural variant calling and phasing using Oxford nanopore sequencing
Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data