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multi-ancestry fine-mapping pipeline.

Project description

credtools

pypi python Build Status codecov License: MIT

Multi-ancestry fine-mapping pipeline.

Features

  • Whole-genome preprocessing: Start from raw GWAS summary statistics and genotype data
    • Standardize and munge summary statistics from various formats
    • Prepare LD matrices and fine-mapping inputs automatically
  • Multi-ancestry fine-mapping: Support for multiple fine-mapping tools (SuSiE, FINEMAP, etc.)
  • Meta-analysis capabilities: Combine results across populations and cohorts
  • Quality control: Built-in QC metrics and visualizations
  • Command-line interface: Easy-to-use CLI for all operations

Installation

Basic Installation

pip install credtools

Install with uv

uv pip install credtools

Quick Start

Command Line Usage

# Complete workflow: from whole-genome data to fine-mapping results
# Step 1: Standardize summary statistics
credtools munge raw_gwas_eur.txt,raw_gwas_asn.txt output/munged/

# Step 2: Identify independent loci and chunk data
credtools chunk output/munged/*.munged.txt.gz output/chunks/

# Step 3: Prepare LD matrices and final inputs
credtools prepare output/chunks/chunk_info.txt genotype_config.json output/prepared/

# Step 4: Run fine-mapping pipeline
credtools pipeline output/prepared/final_loci_list.txt output/results/

Preprocessing Workflow

credtools now supports starting from whole-genome summary statistics and genotype data, eliminating the need for manual preprocessing:

Step 1: Munge Summary Statistics (credtools munge)

  • Purpose: Standardize and clean GWAS summary statistics from various formats
  • Features:
    • Automatic header detection and mapping
    • Data validation and quality control
    • Support for multiple file formats
  • Input: Raw GWAS files with various column headers
  • Output: Standardized .munged.txt.gz files

Step 2: Chunk Loci (credtools chunk)

  • Purpose: Identify independent loci and create regional chunks for fine-mapping
  • Features:
    • Distance-based independent SNP identification
    • Cross-ancestry loci coordination
    • Configurable significance thresholds
  • Input: Munged summary statistics files
  • Output: Locus-specific chunked files and metadata

Step 3: Prepare Inputs (credtools prepare)

  • Purpose: Generate LD matrices and final fine-mapping input files
  • Features:
    • LD matrix computation from genotype data
    • Variant intersection and quality control
    • Multi-threaded processing
  • Input: Chunked files + genotype data configuration
  • Output: credtools-ready input files (.sumstats.gz, .ld.npz, .ldmap.gz)

Multi-Ancestry Support

  • Consistent loci definition: Union approach across ancestries
  • Flexible input formats: Support for various GWAS summary statistics formats
  • Coordinated processing: Ensure compatibility across populations

Documentation

For detailed documentation, see https://Jianhua-Wang.github.io/credtools

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