- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2156
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Progress in methods for rare variant association ; volume:17 ; number:2 ; day:3 ; month:2 ; year:2016 ; pages:57-66 ; date:12.2016
BMC genetics ; 17, Heft 2 (3.2.2016), 57-66, 12.2016
- Urheber
-
Santorico, Stephanie A.
- Beteiligte Personen und Organisationen
-
Hendricks, Audrey E.
SpringerLink (Online service)
- DOI
-
10.1186/s12863-015-0316-7
- URN
-
urn:nbn:de:1111-201608025999
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:45 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Santorico, Stephanie A.
- Hendricks, Audrey E.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Identifying Rare Variant Associations in Admixed Populations
Small sample properties of rare variant analysis methods
Evaluating methods for combining rare variant data in pathway-based tests of genetic association
Integration of variant annotations using deep set networks boosts rare variant association testing
A biologically informed method for detecting rare variant associations
Evaluation of pooled association tests for rare variant identification
Family-based Bayesian collapsing method for rare-variant association study
Comparing family-based rare variant association tests for dichotomous phenotypes
AP-SKAT: highly-efficient genome-wide rare variant association test
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
Identifying rare variant associations in population-based and family-based designs
Rare variant associations with plasma protein levels in the UK Biobank
Identifying Rare Variant Associations in Admixed Populations
Small sample properties of rare variant analysis methods
Evaluating methods for combining rare variant data in pathway-based tests of genetic association
Integration of variant annotations using deep set networks boosts rare variant association testing
A biologically informed method for detecting rare variant associations
Evaluation of pooled association tests for rare variant identification
Family-based Bayesian collapsing method for rare-variant association study
Comparing family-based rare variant association tests for dichotomous phenotypes
AP-SKAT: highly-efficient genome-wide rare variant association test
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
Identifying rare variant associations in population-based and family-based designs
Rare variant associations with plasma protein levels in the UK Biobank
Identifying Rare Variant Associations in Admixed Populations
Small sample properties of rare variant analysis methods
Evaluating methods for combining rare variant data in pathway-based tests of genetic association
Integration of variant annotations using deep set networks boosts rare variant association testing
A biologically informed method for detecting rare variant associations
Evaluation of pooled association tests for rare variant identification
Family-based Bayesian collapsing method for rare-variant association study
Comparing family-based rare variant association tests for dichotomous phenotypes
AP-SKAT: highly-efficient genome-wide rare variant association test
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
Identifying rare variant associations in population-based and family-based designs