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Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux
Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux 
Details Information:
$149.99
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux 
Details Information:
$149.99
Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Python [Complete Training]
Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Python [Complete Training] 
Details Information:
$262.49

Summary

Product Subtotal
Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux  × 1
Details Information:
$149.99
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux  × 1
Details Information:
$149.99
Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Python [Complete Training]  × 1
Details Information:
$262.49
Subtotal $562.47
Total $562.47

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