An integrative variant analysis suite for whole exome next-generation sequencing data
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
An integrative variant analysis suite for whole exome next-generation sequencing data ; volume:13 ; number:1 ; day:12 ; month:1 ; year:2012 ; pages:1-12 ; date:12.2012
BMC bioinformatics ; 13, Heft 1 (12.1.2012), 1-12, 12.2012
- Urheber
-
Challis, Danny
- Beteiligte Personen und Organisationen
-
Yu, Jin
Evani, Uday S.
Jackson, Andrew R.
Paithankar, Sameer
Coarfa, Cristian
Milosavljevic, Aleksandar
Gibbs, Richard A.
Yu, Fuli
SpringerLink (Online service)
- DOI
-
10.1186/1471-2105-13-8
- URN
-
urn:nbn:de:1111-2016021734599
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:21 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Challis, Danny
- Yu, Jin
- Evani, Uday S.
- Jackson, Andrew R.
- Paithankar, Sameer
- Coarfa, Cristian
- Milosavljevic, Aleksandar
- Gibbs, Richard A.
- Yu, Fuli
- SpringerLink (Online service)
Ähnliche Objekte (12)
Next-generation sequencing algorithms : from read mapping to variant detection
Next-generation sequencing algorithms : from read mapping to variant detection
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
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Barcode-free next-generation sequencing error validation for ultra-rare variant detection
Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses
Next-Generation Macrolide Antibiotics
Next-generation human genetics
Next-generation pathogen genomics
Next-generation human genetics
Next-generation sequencing algorithms : from read mapping to variant detection
Next-generation sequencing algorithms : from read mapping to variant detection
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
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Barcode-free next-generation sequencing error validation for ultra-rare variant detection
Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses
Next-Generation Macrolide Antibiotics
Next-generation human genetics
Next-generation pathogen genomics
Next-generation human genetics
Next-generation sequencing algorithms : from read mapping to variant detection
Next-generation sequencing algorithms : from read mapping to variant detection
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
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Barcode-free next-generation sequencing error validation for ultra-rare variant detection
Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses
Next-Generation Macrolide Antibiotics
Next-generation human genetics
Next-generation pathogen genomics