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Genome-wide association study of susceptibility loci for breast cancer in Sardinian population.

BMC cancer | 2015

Despite progress in identifying genes associated with breast cancer, many more risk loci exist. Genome-wide association analyses in genetically-homogeneous populations, such as that of Sardinia (Italy), could represent an additional approach to detect low penetrance alleles.

Pubmed ID: 25956309 RIS Download

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: CA128978
  • Agency: Cancer Research UK, United Kingdom
    Id: C5047/A10692
  • Agency: NIA NIH HHS, United States
    Id: N01-AG-1-2109
  • Agency: NCI NIH HHS, United States
    Id: 1 U19 CA148065-01
  • Agency: NCI NIH HHS, United States
    Id: 1U19 CA148065
  • Agency: Cancer Research UK, United Kingdom
    Id: C5047/A8384
  • Agency: Cancer Research UK, United Kingdom
    Id: C12292/A11174
  • Agency: NCI NIH HHS, United States
    Id: R01 CA128978
  • Agency: NCI NIH HHS, United States
    Id: CA148537
  • Agency: Canadian Institutes of Health Research, Canada
  • Agency: NCI NIH HHS, United States
    Id: U19 CA148537
  • Agency: Cancer Research UK, United Kingdom
    Id: C1287/A 10710
  • Agency: NCI NIH HHS, United States
    Id: 1U19 CA148112
  • Agency: Cancer Research UK, United Kingdom
    Id: C1281/A12014
  • Agency: NCI NIH HHS, United States
    Id: U19 CA148112
  • Agency: NCI NIH HHS, United States
    Id: U19 CA148065
  • Agency: Cancer Research UK, United Kingdom
    Id: C1287/A10118
  • Agency: Cancer Research UK, United Kingdom
    Id: C5047/A15007

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This is a list of tools and resources that we have found mentioned in this publication.


METAL (tool)

RRID:SCR_002013

Software application designed to facilitate meta-analysis of large datasets (such as several whole genome scans) in a convenient, rapid and memory efficient manner. (entry from Genetic Analysis Software)

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Eigensoft (tool)

RRID:SCR_004965

EIGENSOFT package combines functionality from our population genetics methods (Patterson et al. 2006) and our EIGENSTRAT stratification method (Price et al. 2006). The EIGENSTRAT method uses principal components analysis to explicitly model ancestry differences between cases and controls along continuous axes of variation; the resulting correction is specific to a candidate marker''s variation in frequency across ancestral populations, minimizing spurious associations while maximizing power to detect true associations. The EIGENSOFT package has a built-in plotting script and supports multiple file formats and quantitative phenotypes. Source code, documentation and executables for using EIGENSOFT 3.0 on a Linux platform can be downloaded. New features of EIGENSOFT 3.0 include supporting either 32-bit or 64-bit Linux machines, a utility to merge different data sets, a utility to identify related samples (accounting for population structure), and supporting multiple file formats for EIGENSTRAT stratification correction.

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RELPAIR (tool)

RRID:SCR_009358

Software program that infers the relationships of pairs of individuals based on genetic marker data, either within families or across an entire sample. (entry from Genetic Analysis Software)

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SNPTEST (tool)

RRID:SCR_009406

Software program for the analysis of single SNP association in genome-wide studies. The tests implemented can cater for binary (case-control) and quantitative phenotypes, can condition upon an arbitrary set of covariates and properly account for the uncertainty in genotypes. The program is designed to work seamlessly with the output of both the genotype calling program CHIAMO, the genotype imputation program IMPUTE and the program GTOOL. This program was used in the analysis of the 7 genome-wide association studies carried out by the Wellcome Trust Case-Control Consortium (WTCCC). (entry from Genetic Analysis Software)

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MACH (tool)

RRID:SCR_009621

QTL analysis based on imputed dosages/posterior_probabilities.

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IMPUTE2 (tool)

RRID:SCR_013055

A computer program for phasing observed genotypes and imputing missing genotypes.

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