QTLtools-gwas(1) | Bioinformatics tools | QTLtools-gwas(1) |
QTLtools gwas - Genome-wide association tests
QTLtools gwas --vcf [in.vcf|in.vcf.gz|in.bcf|in.bed.gz] --bed quantifications.bed.gz --out output.txt [OPTIONS]
This mode runs a linear regression with every genotype vs. every phenotype.
1 | The phenotype ID |
2 | The variant's chromosome |
3 | The variants's start position |
3.1 | The variant's end position. Only printed if a BED file is supplied to --vcf |
4 | The variant's ID |
5 | The p-value |
6 | The correlation coefficient |
QTLtools website: <https://qtltools.github.io/qtltools>
Versions up to and including 1.2, suffer from a bug in reading missing genotypes in VCF/BCF files. This bug affects variants with a DS field in their genotype's FORMAT and have a missing genotype (DS field is .) in one of the samples, in which case genotypes for all the samples are set to missing, effectively removing this variant from the analyses.
Please submit bugs to <https://github.com/qtltools/qtltools>
Delaneau O., Ongen H., Brown A. A., et al. A complete tool set for molecular QTL discovery and analysis. Nat Commun 8, 15452 (2017). <https://doi.org/10.1038/ncomms15452>
Olivier Delaneau (olivier.delaneau@gmail.com), Halit Ongen (halitongen@gmail.com)
06 May 2020 | QTLtools-v1.3 |