A collection of handy tools for GWAS
Project description
A collection of handy python scripts for GWAS. Just want to make life eaiser and save myself from repetitive work.
For usage, please check GWASLab document at https://cloufield.github.io/gwaslab/ .
What you can do with gwaslab:
Standardization, Normalization & Harmonization
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CHR and POS notation standardization
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Variant POS and allele normalization
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Genome build : Liftover
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Reference allele alignment using a reference genome sequence
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rsID assignment based on CHR, POS, REF and ALT
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CHR POS assignment based on rsID using a reference VCF
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Palindromic SNPs and indels strand inference using a reference VCF
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Check allele frequency discrepancy using a reference VCF
Quality control, Value conversion & Filtering
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Statistics sanity check
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Equivalent statistics conversion
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BETA/SE , OR/OR_95L/OR_95U
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P, Z, CHISQ, MLOG10
-
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Extract/exclude hapmap3 variants
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Extract/exclude MHC variants
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Filtering values.
Visualization
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Mqq plot : Manhattan plot and QQ plot side by side
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Heatmap : ldsc-rg genetic correlation matrix
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Scatter Plot : variant effect size comparison with sumstats
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Scatter Plot : allele frequency comparison
Other Utilities
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Read ldsc h2 or rg outputs directly as DataFrames
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Extract lead SNPs given a window size
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Logging : keep a complete record of manipulations from raw data to munged data
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Formating GWAS sumstats in certain formats
- LDSC / MAGMA / METAL / MR-MEGA / FUMA ...
Requirements
- Python >= 3
- pyVCF >= 0.6.8
- Biopython >= 1.79
- liftover >= 1.1.13
- pandas >= 1.2.4
- numpy >= 1.21.2
- matplotlib>3.5
- seaborn >= 0.11.1
- scipy >= 1.6.2
- adjustText
Install
pip install gwaslab
Current version: 3.0.0
Usage
For usage, please check GWASLab document at https://cloufield.github.io/gwaslab/ .
Update Log
-
3.0.0 first complete version
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1.0.0 implemented Sumstats object
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0.0.5 - 0.0.6
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added compare_effect, read_ldsc
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0.0.4
- added mqqplot feature
- fixed gtesig algorithm
- recreated mplot and qqplot
For more information: https://gwaslab.com/
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