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docs: add Analysis methopds draft
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berntpopp committed May 30, 2024
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## Methods {-}

### Sample selection and preparation

### Analysis of sequencing data
We implemented a comprehensive workflow for aligning, calling variants, and annotating sequencing data. The raw sequencing data files were obtained from the sequencing provider in FASTQ format. The BWA (Burrows-Wheeler Aligner) tool was used to align the sequences to the hg38 the reference genome. The GATK (Genome Analysis Toolkit) was used for variant calling. We used SnpEff and SnpSift to perform annotations. The GitHub repository contains detailed instructions as well as the complete codebase.

## Results {-}



## Conclusion {-}



## Outlook {-}

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