A combined association test for rare variants using family and case-control data

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1753-6561

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: A combined association test for rare variants using family and case-control data ; volume:10 ; number:7 ; day:18 ; month:10 ; year:2016 ; pages:215-219 ; date:10.2016
BMC proceedings / Biomed Central ; 10, Heft 7 (18.10.2016), 215-219, 10.2016

Creator: Lin, Peng-Lin

Contributor: Tsai, Wei-Yun
Chung, Ren-Hua
SpringerLink (Online service)

DOI: 10.1186/s12919-016-0033-x

URN: urn:nbn:de:1111-201701036358

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 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

Lin, Peng-Lin
Tsai, Wei-Yun
Chung, Ren-Hua
SpringerLink (Online service)

Other Objects (12)

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

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.

A combined association test for rare variants using family and case-control data

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

A novel method to detect rare variants using both family and unrelated case-control data

Genome-wide case-control study in GAW17 using coalesced rare variants

Family- and population-based designs identify different rare causal variants

Family studies to find rare high risk variants in migraine

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Prioritization of family member sequencing for the detection of rare variants

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates

Application of family-based tests of association for rare variants to pathways

Family-based tests applied to extended pedigrees identify rare variants related to hypertension

Testing rare variants for hypertension using family-based tests with different weighting schemes

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

Related objects

Reset password