CandiSNPer: A web tool for the identification of candidate SNPs for causal variants

Bioinformatics

Volumn 26, Issue 7, 2010, Pages 969-970

  Schmitt, Armin O ^a   Aßmus, Jens ^a   Bortfeldt, Ralf H ^a   Brockmann, Gudrun A ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

APIS;

ARTICLE; COMPUTER PROGRAM; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOMICS; GENOTYPE; INTERNET; METHODOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM;

GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; GENOTYPE; INTERNET; POLYMORPHISM, SINGLE NUCLEOTIDE; SOFTWARE;

EID: 77951959817     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btq068     Document Type: Article

References (5)

1. Cooper, G.M. et al. (2005) Distribution and intensity of constraint in mammalian genomic sequence. Genome Res., 15, 901-913.
2. Hindorff, L.A. et al. (2009)Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. USA, 106, 9362-9367.
3. Johnson, A.D. et al. (2008)SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics, 24, 2938-2939.
4. Sandhu, M.S. et al. (2008) LDL-cholesterol concentrations: a genome-wide association study. Lancet, 371, 483-491.
5. Thorisson, G.A. et al. (2005) The International HapMap Project Web site. Genome Res., 15, 1592-1593.