BioConductor
GWASTools 1.26.1
Tools for Genome Wide Association Studies
Released May 24, 2018 by Stephanie M. Gogarten
Dependencies
DBI 1.0.0 DNAcopy 1.54.0 sandwich 2.4-0 quantsmooth 1.46.0 survival 2.42-3 RSQLite Biobase 2.40.0 logistf 1.22 GWASExactHW 1.01 lmtest 0.9-36 gdsfmt 1.16.0
Classes for storing very large GWAS data sets and annotation, and functions for GWAS data cleaning and analysis.
Installation
Maven
This package can be included as a dependency from a Java or Scala project by including
the following your project's pom.xml
file.
Read more
about embedding Renjin in JVM-based projects.
<dependencies> <dependency> <groupId>org.renjin.bioconductor</groupId> <artifactId>GWASTools</artifactId> <version>1.26.1-b1</version> </dependency> </dependencies> <repositories> <repository> <id>bedatadriven</id> <name>bedatadriven public repo</name> <url>https://nexus.bedatadriven.com/content/groups/public/</url> </repository> </repositories>
Renjin CLI
If you're using Renjin from the command line, you load this library by invoking:
library('org.renjin.bioconductor:GWASTools')
Test Results
This package was last tested against Renjin 0.9.2644 on Jun 2, 2018.
- BAFfromClusterMeans-examples
- GdsGenotypeReader-class-examples
- GdsIntensityReader-class-examples
- GdsReader-class-examples
- GenotypeData-class-examples
- HLA-examples
- IntensityData-class-examples
- MatrixGenotypeReader-class-examples
- NcdfGenotypeReader-class-examples
- NcdfIntensityReader-class-examples
- NcdfReader-class-examples
- ScanAnnotationDataFrame-class-examples
- ScanAnnotationSQLite-class-examples
- SnpAnnotationDataFrame-class-examples
- SnpAnnotationSQLite-class-examples
- alleleFrequency-examples
- allequal-examples
- anomDetectBAF-examples
- anomDetectLOH-examples
- anomIdentifyLowQuality-examples
- anomSegStats-examples
- apartSnpSelection-examples
- assocCoxPH-examples
- assocRegression-examples
- batchTest-examples
- centromeres-examples
- chromIntensityPlot-examples
- convertNcdfGds-examples
- createDataFile-examples
- duplicateDiscordance-examples
- duplicateDiscordanceAcrossDatasets-examples
- duplicateDiscordanceProbability-examples
- exactHWE-examples
- findBAFvariance-examples
- gdsSubset-examples
- genoClusterPlot-examples
- genotypeToCharacter-examples
- getobj-examples
- hetByScanChrom-examples
- hetBySnpSex-examples
- ibdPlot-examples
- imputedDosageFile-examples
- intensityOutliersPlot-examples
- manhattanPlot-examples
- meanIntensityByScanChrom-examples
- mendelErr-examples
- mendelList-examples
- missingGenotypeByScanChrom-examples
- missingGenotypeBySnpSex-examples
- pasteSorted-examples
- pcaSnpFilters-examples
- pedigreeCheck-examples
- pedigreeDeleteDuplicates-examples
- pedigreeMaxUnrelated-examples
- pedigreePairwiseRelatedness-examples
- plinkUtils-examples
- pseudoautoIntensityPlot-examples
- pseudoautosomal-examples
- qqPlot-examples
- qualityScoreByScan-examples
- qualityScoreBySnp-examples
- readWriteFirst-examples
- relationsMeanVar-examples
- saveas-examples
- setMissingGenotypes-examples
- simulateGenotypeMatrix-examples
- snpCorrelationPlot-examples
- snpStats-examples
- test
- vcfWrite-examples