The TruSight Cardio Sequencing Kit is a comprehensive, cost-effective solution for identifying causal variants implicated in Inherited Cardiac Conditions (ICCs). The panel content is designed with expertly defined genes selected in collaboration with the Imperial College of London. 99% of the targeted regions are covered at a depth of at least 20x. The cost to sequence is ~$1 US per gene and is fully supported on Illumina industry-leading sequencing and informatics platforms.
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| * Library prep is compatible with all Illumina instruments. Recommended instruments chosen based on typical output and analysis need for selected application. † Based on 300x mean coverage of targeted content. |
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| Project Recommendations | ||||
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| Species Compatibility | Human | |||
| Recommended Illumina Instrument* | MiSeq | NextSeq 500 | ||
| Run Mode | - | Mid Output | ||
| Recommended Samples per run† | 12 (v2 chemistry) | 48 | ||
| Max Recommended Read Length | 2x150 bp | 2x150 bp | ||
| Recommended Secondary Analysis |
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| Recommended Down Stream Analysis | VariantStudio | VariantStudio | ||