How to use the Illumina® Sequencing Coverage Calculator

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In this video, we will walk through using the Illumina™ Sequencing Coverage Calculator to determine the number of samples per MiniSeq™ or NovaSeq™ 6000 run. We’ll go through specific examples for whole-genome sequencing (WGS), custom DNA content, total RNA-Seq, and a pre-defined panel: the AmpliSeq™ for Illumina Focus panel.

To access the Illumina Sequencing Coverage Calculator, please visit: 

The methods and tools depicted in this video are for research use only and not for use in diagnostic procedures.

©2021 Illumina, Inc. All Rights Reserved.
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A global genomics leader, Illumina provides comprehensive next-generation sequencing solutions to the research, clinical, and applied markets. Illumina technology is responsible for generating more than 90% of the world’s sequencing data.* Through collaborative innovation, Illumina is fueling groundbreaking advancements in oncology, reproductive health, genetic disease, microbiology, agriculture, forensic science, and beyond.

*Data calculations on file. Illumina, Inc., 2015.

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Nothing like deep vibes chillwave while calculating sequence coverage.

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