Effective normalization for copy number variation detection from whole genome sequencing

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2164

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Effective normalization for copy number variation detection from whole genome sequencing ; volume:13 ; number:6 ; day:26 ; month:10 ; year:2012 ; pages:1-11 ; date:10.2012
BMC genomics ; 13, Heft 6 (26.10.2012), 1-11, 10.2012

Creator: Janevski, Angel

Contributor: Varadan, Vinay
Kamalakaran, Sitharthan
Banerjee, Nilanjana
Dimitrova, Nevenka
SpringerLink (Online service)

DOI: 10.1186/1471-2164-13-S6-S16

URN: urn:nbn:de:1111-2016072840830

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:59 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Janevski, Angel
Varadan, Vinay
Kamalakaran, Sitharthan
Banerjee, Nilanjana
Dimitrova, Nevenka
SpringerLink (Online service)

Other Objects (12)

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Effective normalization for copy number variation detection from whole genome sequencing

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

ACEseq – allele specific copy number estimation from whole genome sequencing

Sacral agenesis: a pilot whole exome sequencing and copy number study

ECOLE: Learning to call copy number variants on whole exome sequencing data

Comparative study of whole exome sequencing-based copy number variation detection tools

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Normalization of array-CGH data: influence of copy number imbalances

Effective normalization for copy number variation in Hi-C data

Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

Related objects

Reset password