Variant Set Enrichment: an R package to identify disease-associated functional genomic regions
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-0381
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Variant Set Enrichment: an R package to identify disease-associated functional genomic regions ; volume:10 ; number:1 ; day:22 ; month:2 ; year:2017 ; pages:1-5 ; date:12.2017
BioData Mining ; 10, Heft 1 (22.2.2017), 1-5, 12.2017
- Schlagwort
-
Krebs
Onkologie
- Urheber
-
Ahmed, Musaddeque
- Beteiligte Personen und Organisationen
-
Sallari, Richard C.
Guo, Haiyang
Moore, Jason H.
He, Housheng Hansen
Lupien, Mathieu
SpringerLink (Online service)
- DOI
-
10.1186/s13040-017-0129-5
- URN
-
urn:nbn:de:1111-201703231170
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:57 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
- Ahmed, Musaddeque
- Sallari, Richard C.
- Guo, Haiyang
- Moore, Jason H.
- He, Housheng Hansen
- Lupien, Mathieu
- SpringerLink (Online service)
Ähnliche Objekte (12)
Reversible mislocalization of a disease-associated MRE11 splice variant product
Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
Disease-associated HCN4 V759I variant is not sufficient to impair cardiac pacemaking
The Alzheimer’s disease-associated protective Plcγ2-P522R variant promotes immune functions
Acorn: an R package for de novo variant analysis
satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect
Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene
ORdensity: user-friendly R package to identify differentially expressed genes
Regulatory landscape enrichment analysis (RLEA): a computational toolkit for non-coding variant enrichment and cell type prioritization
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
GSEPD: a Bioconductor package for RNA-seq gene set enrichment and projection display
CVE: an R package for interactive variant prioritisation in precision oncology
Reversible mislocalization of a disease-associated MRE11 splice variant product
Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
Disease-associated HCN4 V759I variant is not sufficient to impair cardiac pacemaking
The Alzheimer’s disease-associated protective Plcγ2-P522R variant promotes immune functions
Acorn: an R package for de novo variant analysis
satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect
Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene
ORdensity: user-friendly R package to identify differentially expressed genes
Regulatory landscape enrichment analysis (RLEA): a computational toolkit for non-coding variant enrichment and cell type prioritization
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
GSEPD: a Bioconductor package for RNA-seq gene set enrichment and projection display
CVE: an R package for interactive variant prioritisation in precision oncology
Reversible mislocalization of a disease-associated MRE11 splice variant product
Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
Disease-associated HCN4 V759I variant is not sufficient to impair cardiac pacemaking
The Alzheimer’s disease-associated protective Plcγ2-P522R variant promotes immune functions
Acorn: an R package for de novo variant analysis
satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect
Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene
ORdensity: user-friendly R package to identify differentially expressed genes
Regulatory landscape enrichment analysis (RLEA): a computational toolkit for non-coding variant enrichment and cell type prioritization
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
GSEPD: a Bioconductor package for RNA-seq gene set enrichment and projection display