Basic information
Homepage
Download & Installation
Compilation examples
GitHub / QTLtools
QTLtools figures
Analyses
Preparing input files
Overview of QTLtools
[bamstat]
QC the sequence data
[mbv]
Sequence to genotype matching
[quan]
Quantify gene expression
[pca]
Perform PCA on data
[cis]
Discover QTL in
cis
[nominal pass]
[cis]
Discover QTL in
cis
[permutation pass]
[cis]
Discover QTL in
cis
[conditional pass]
[trans]
Discover QTL in
trans
[full pass]
[trans]
Discover QTL in
trans
[approx. pass]
[fdensity]
Annotation density at QTLs
[fenrich]
Enrichment of QTLs in annotations
[rtc]
Overlap QTLs with GWAS hits
Man Pages
Overview of QTLtools
[bamstat]
Calculate basic QC metrics for BAM/SAM
[mbv]
Sequence to genotype matching
[pca]
Perform PCA on data
[correct]
Covariate correction of BED or VCF file
[cis]
Discover QTL in
cis
[trans]
Discover QTL in
trans
[fenrich]
Enrichment of QTLs in annotations
[fdensity]
Annotation density at QTLs
[rtc]
Colocalization analysis of QTLs and GWAS hits
[rtc-union]
Find the union of QTLs
[extract]
Extract all data from the provided files
[quan]
Quantify gene and exon expression
[ase]
Measure allele specific expression
[rep]
Replicate QTLs in an independent dataset
[gwas]
Correlate all genotypes with all phenotypes
Credits
Dr Olivier DELANEAU, UNIGE
Dr Halit ONGEN, UNIGE
Prof. Manolis DERMITZAKIS, UNIGE
References
QTLtools: a complete tool set for molecular QTL discovery and analysis.
Nat Commun
8
, 15452 (2017).
Estimating the causal tissues for complex traits and diseases.
Nat Genet.
2017;
49
(12):1676-1683.
MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets.
Bioinformatics
33
(12), 1895 2017.