I will process and analyze your genomics or vcf data using python

Do you have genomics data that needs processing, filtering, or 

annotation but don't know where to start?

I will build a reliable bioinformatics pipeline to process your 

VCF, BCF, or GWAS data using industry-standard tools delivering 

clean, annotated, analysis-ready results.

What I can do:

VCF/BCF file processing and format conversion

Variant filtering by quality, depth, and allele frequency

SNP annotation using Ensembl VEP

PLINK-based GWAS data processing

bcftools QC stats and summary reports

File format conversions (VCF, BCF, PLINK, haps/sample)

Python automation of full pipeline workflows

Data visualization of variant distributions and quality metrics

What you'll receive:

Processed, filtered output files

QC summary report

Python pipeline script (clean, commented, reusable)

Clear documentation and usage instructions

I work with bcftools, tabix, PLINK, Ensembl VEP, and Python 

the same tools used in production GWAS and genomics research pipelines.

Message me before ordering to describe your dataset and goals.