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bioinformatics data scientist
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Bioinformatics
Workflow of BioInfo
- Base Calling
- Aligment
- Variant Calling
- Filtering / Annotation
- Casual Variants
Process: Sequence Signal to Nucleotides
Result: FASTQ-large number of short reads
Process: Aligning to the reads to the reference of genomes
Result: SAM/BAM - Aligment file
Process: Obsesrve differences of sample from references
Result: VCF - List of variants
Process: Database lookup of variants & filterling
Result: Small anotaitates list of variants
Process: Identyfing most promissing candidates variants
Result: Casual variants
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