A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-994X
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data ; volume:12 ; number:1 ; day:30 ; month:1 ; year:2020 ; pages:1-11 ; date:12.2020
Genome medicine ; 12, Heft 1 (30.1.2020), 1-11, 12.2020
- Creator
-
Rajagopalan, Ramakrishnan
Murrell, Jill R.
Luo, Minjie
Conlin, Laura K.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13073-020-0712-0
- URN
-
urn:nbn:de:101:1-2020050203512375550955
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 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
- Rajagopalan, Ramakrishnan
- Murrell, Jill R.
- Luo, Minjie
- Conlin, Laura K.
- SpringerLink (Online service)
Other Objects (12)
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
Inferring copy number and genotype in tumour exome data
Assessing the reproducibility of exome copy number variations predictions
Identification of copy number variants from exome sequence data
Sacral agenesis: a pilot whole exome sequencing and copy number study
Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome
Comparative study of whole exome sequencing-based copy number variation detection tools
ECOLE: Learning to call copy number variants on whole exome sequencing data
CoNVEX: copy number variation estimation in exome sequencing data using HMM
Intelligent workflow : support for context sensitive business process modelling
A Bayesian change-point algorithm for detecting copy number alteration
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
Inferring copy number and genotype in tumour exome data
Assessing the reproducibility of exome copy number variations predictions
Identification of copy number variants from exome sequence data
Sacral agenesis: a pilot whole exome sequencing and copy number study
Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome
Comparative study of whole exome sequencing-based copy number variation detection tools
ECOLE: Learning to call copy number variants on whole exome sequencing data
CoNVEX: copy number variation estimation in exome sequencing data using HMM
Intelligent workflow : support for context sensitive business process modelling
A Bayesian change-point algorithm for detecting copy number alteration
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
Inferring copy number and genotype in tumour exome data
Assessing the reproducibility of exome copy number variations predictions
Identification of copy number variants from exome sequence data
Sacral agenesis: a pilot whole exome sequencing and copy number study
Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome
Comparative study of whole exome sequencing-based copy number variation detection tools
ECOLE: Learning to call copy number variants on whole exome sequencing data
CoNVEX: copy number variation estimation in exome sequencing data using HMM
Intelligent workflow : support for context sensitive business process modelling