Whole Genome Sequencing Data Analysis

I need a comprehensive analysis of whole genome sequencing data. The analysis should include variant calling (SNPs, Indels, SVs), functional annotation, and a report on medical implications.

Key requirements:
- Variant calling using Manta for structural variants
- Expertise in SNPs, Indels, and SVs
- Functional annotation of variants
- Detailed medical implications report

Ideal skills and experience:
- Proficiency in genomic data analysis
- Familiarity with Manta and other variant calling tools
- Strong background in bioinformatics and genomics
- Ability to interpret and report on medical relevance of genetic variants

**I have attached a preview of the data**

Please provide relevant experience in your bids.