Comment on 'discrepancies in dbSNP confirmations rates and allele frequency distributions from varying genotyping error rates and patterns'

Bioinformatics

Volumn 21, Issue 2, 2005, Pages 141-143

  Carlson, Christopher S ^a   Reider, Mark J ^a   Nickerson, Deborah A ^a   Eberle, Michael A ^b,c   Kruglyak, Leonid ^b,c  

^a UNIVERSITY OF WASHINGTON   (United States)

^b Fred Hutchinson Cancer Research Center   (United States)

^c HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACCESS TO INFORMATION; ALLELE; ANALYTICAL ERROR; CHROMOSOME ANALYSIS; EDITORIAL; GENE FREQUENCY; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; INFORMATION PROCESSING; PREDICTION; PRIORITY JOURNAL; PROBABILITY; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 13444302836     PISSN: 13674803     EISSN: 13674811     Source Type: Journal    
DOI: 10.1093/bioinformatics/bth492     Document Type: Editorial

References (6)

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2. Carlson,C.S., Eberle,M.A., Rieder,M.J., Smith,J.D., Kruglyak,L. and Nickerson,D.A. (2003) Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans. Nat. Genet., 33, 518-521.
3. Hudson,R.R. (2002) Generating samples under a Wright-Fisher neutral model of genetic variation. Bioinformatics, 18, 337-338.
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