ゲノミクスを簡素化するMiniSeqリソース

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MiniSeqリソース

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製品選択ツールおよび実験計画ツール
MiniSeq User Guide

This guide contains an overview of instrument components and instructions for operating and maintaining the MiniSeq System.

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Sequencing Coverage

Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.

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Quality Scores

Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.

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Custom Protocol Selector

The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.

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Proven Illumina NGS, Now More Accessible Than Ever
Proven Illumina NGS, Now More Accessible Than Ever

Discover how the simple, affordable MiniSeq System makes sequencing an everyday tool for labs of any size.

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Go Mini Scientific Challenge 1st Place Winner
Go Mini Scientific Challenge 1st Place Winner

Mattia Prosperi, PhD, will use his MINI Cooper and MiniSeq to study the spread of mosquito-borne pathogens in Florida.

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Go Mini Scientific Challenge 2nd Place Winner
Go Mini Scientific Challenge 2nd Place Winner

Hongmei Li-Byarlay, PhD, describes how she will use the MiniSeq to study the honeybee.

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Go Mini Scientific Challenge 3rd Place Winner
Go Mini Scientific Challenge 3rd Place Winner

Una McVeigh discusses how the MiniSeq System will help her identify new genetic variants associated with breast cancer.

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MiniSeq System Demonstration
MiniSeq System Demonstration

This webinar provides an introduction to the MiniSeq System and its simple, streamlined workflow.

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Adopting NGS for Tumor Profiling
Adopting NGS for Tumor Profiling

Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.

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