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Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux 
$149.99
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Hands-on: NGS (Whole Exome) Variant Calling Using Python
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Python 
$187.49
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Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux
Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux 
$149.99
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Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux
Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux 
$149.99
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Summary

Subtotal $637.46
Learning path bundle — NGS & variant calling (30% off) - $191.24
Total $446.22
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