Improving somatic variant identification through integration of genome and exome data

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2164

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Improving somatic variant identification through integration of genome and exome data ; volume:18 ; number:7 ; day:16 ; month:10 ; year:2017 ; pages:63-71 ; date:10.2017
BMC genomics ; 18, Heft 7 (16.10.2017), 63-71, 10.2017

Classification: Biowissenschaften, Biologie

Creator: Vijayan, Vinaya

Contributor: Yiu, Siu-Ming
Zhang, Liqing
SpringerLink (Online service)

DOI: 10.1186/s12864-017-4134-3

URN: urn:nbn:de:1111-2017121120559

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:39 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

Vijayan, Vinaya
Yiu, Siu-Ming
Zhang, Liqing
SpringerLink (Online service)

Other Objects (12)

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

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.

Improving somatic variant identification through integration of genome and exome data

Object Details

References and Relationships

Classification and Topics

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic exome sequencing performance by biological replicates

Correction: Improving somatic exome sequencing performance by biological replicates

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Variant detection sensitivity and biases in whole genome and exome sequencing

Genome-wide somatic variant calling using localized colored de Bruijn graphs

SomaticCombiner: improving the performance of somatic variant calling based on evaluation tests and a consensus approach

Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection

Quantifying single nucleotide variant detection sensitivity in exome sequencing

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Related objects

Reset password