Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1753-6561

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals ; volume:10 ; number:7 ; day:18 ; month:10 ; year:2016 ; pages:203-207 ; date:10.2016
BMC proceedings / Biomed Central ; 10, Heft 7 (18.10.2016), 203-207, 10.2016

Creator: Darst, Burcu F.

Contributor: Engelman, Corinne D.
SpringerLink (Online service)

DOI: 10.1186/s12919-016-0031-z

URN: urn:nbn:de:1111-201701036580

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:55 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

Darst, Burcu F.
Engelman, Corinne D.
SpringerLink (Online service)

Other Objects (12)

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

$Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller$

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

$Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller$

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

$Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller$

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome 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.

Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

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

Red panda: a novel method for detecting variants in single-cell RNA sequencing

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller

Detecting molecules in Ariel low resolution transmission spectra

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Whole-genome sequencing data of Kazakh individuals

Detecting antibody reactivities in Phage ImmunoPrecipitation Sequencing data

Detecting complex infections in trypanosomatids using whole genome sequencing

JAFFAL: detecting fusion genes with long-read transcriptome sequencing

Related objects

Reset password