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Check GWAS Inputs (version 2.0.0)
Allelic file in Hapmap format
Phenotypic file

Authors South Green

Please cite "SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations", Dereeper A. et al., Nucl. Acids Res. (1 july 2015) 43 (W1).

Galaxy integration Provided by Southgreen & Dereeper Alexis (IRD) & Marcon Valentin (IFB & INRA)

Support For any questions about Galaxy integration, please send an e-mail to alexis.dereeper@ird.fr


CheckGWASInputs

Description

CheckGWASInputs checks concordance between input files for GWAS analysis.

Input files

Hapmap file
Allelic file in Hapmap format
Trait file
Phenotypic file

Output files

Hapmap output

Trait output

Logfile and statistics


Working example

Input files

Hapmap file

rs#     alleles chrom   pos     strand  assembly#       center  protLSID        assayLSID       panel   QCcode  Ind1    Ind2
SNP1    A/T     1       3102    +       assembly        NA      NA      NA      speciesname     NA      AA      AA      AA
SNP2    A/T     1       4648    +       assembly        NA      NA      NA      speciesname     NA      AA      AA      AA

Trait file

<Trait> Test
Ind1    -2.9985936006411
Ind2    -2.68669426456267

Output files

Hapmap output

rs#     alleles chrom   pos     strand  assembly#       center  protLSID        assayLSID       panel   QCcode  Ind1    Ind2    Ind3    Ind4
SNP1    A/T     1       3102    +       assembly        NA      NA      NA      speciesname     NA      AA      AA      AA      AA      AA
SNP2    A/T     1       4648    +       assembly        NA      NA      NA      speciesname     NA      AA      AA      AA      AA      TT

Trait output

<Trait> Test
Ind429  -26.2142525264157
Ind373  12.0306115988504
Ind81   1.98118654229534

Logfile and statistics

==============================================
Individuals
==============================================
Individuals in hapmap file: 500
Individuals in trait file: 500
Individuals found in both files: 500
==============================================
Markers
==============================================
Discarded markers:
Monomorphic: 0
Not biallelic: 0
Modified markers:
Difference in variation: 0