Order the NovaSeq X Series
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).
TruSight Cardio enrichment oligos are now available separately for use with Illumina DNA Prep with Enrichment. The TruSight Cardio Sequencing Kit for MiSeq and MiSeqDx (FC-141-1010) and TruSight Cardio Sequencing Kits for NextSeq (FC-141-1011 and 20035190) have been discontinued.
The TruSight Cardiomyopathy Sequencing Panel has been discontinued. The TruSight Cardio Sequencing Kit is the recommended replacement.
The TruSight Cardio Panel uses next-generation sequencing (NGS) to provide comprehensive coverage of 174 genes with known associations to 17 ICCs, including cardiomyopathies, arrhythmias, aortopathies, and more. Genes were expertly selected with researchers at the National Heart Centre Singapore and Imperial College of London. Content includes genes known to be associated with hereditary heart disease and emerging genes found in the literature.1
* Data on file. Illumina, Inc. 2015.
Content specifications | 575 Kb genomic content (174 genes) |
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Description | Targeted sequencing research panel to identify causal variants associated with 17 inherited cardiac conditions. |
Input quantity | 50 ng DNA |
Instruments | MiSeq System, NextSeq 550 System, NextSeq 2000 System, NextSeq 1000 System, MiSeqDx in Research Mode, MiniSeq System, NextSeq 500 System |
Method | Targeted DNA sequencing, Target enrichment |
Multiplexing | Up to 96-plex |
Nucleic acid type | DNA |
Specialized sample types | Not FFPE-compatible |
Species category | Human |
Technology | Sequencing |
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants |
Instrument | Recommended number of samples | Read length |
---|---|---|
MiSeq System | 12 samples per run with v2 reagents (based on 300x mean coverage of targeted content) |
2 × 150 bp (max recommended) |
NextSeq 550 System | 96 samples per run (mid output; based on 300x mean coverage of targeted content) |
2 × 150 bp (max recommended) |
Overview of genomic sequencing for cardiovascular diseases.
With targeted resequencing, a subset of genes or a genomic region is isolated and sequenced, which can conserve lab resources.
TruSight Cardio Sequencing Panel | TruSight One Sequencing Panels | ||||
---|---|---|---|---|---|
Content specifications | 575 Kb genomic content (174 genes) |
TruSight One: ~12 Mb genomic content (~4800 genes). TruSight One Expanded: ~16.5 Mb genomic content (~6700 genes). |
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Description | Targeted sequencing research panel to identify causal variants associated with 17 inherited cardiac conditions. | ||||
Input quantity | 50 ng DNA | 50 ng DNA | |||
Instruments | MiSeq System, NextSeq 550 System, NextSeq 2000 System, NextSeq 1000 System, MiSeqDx in Research Mode, MiniSeq System, NextSeq 500 System | MiSeq System, NextSeq 550 System, NextSeq 2000 System, NextSeq 1000 System, MiSeqDx in Research Mode, MiniSeq System, NextSeq 500 System, NovaSeq 6000 System | |||
Method | Targeted DNA sequencing, Target enrichment | Targeted DNA sequencing, Target enrichment | |||
Multiplexing | Up to 96-plex | Up to 96-plex | |||
Nucleic acid type | DNA | DNA | |||
Specialized sample types | Not FFPE-compatible | Not FFPE-compatible | |||
Species category | Human | Human | |||
Technology | Sequencing | Sequencing | |||
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants | Single nucleotide polymorphisms (SNPs), Germline variants |
Dr. Stuart Cook: Targeted gene analysis with TruSight Cardio Sequencing
Download this reference guide to understand which kit quantities you should purchase to support your research.
TruSight Cardio – Enrichment Oligos only (8 Enrichment Reactions)
20029229
Sufficient for eight enrichment reactions when paired with Illumina DNA Prep with Enrichment. Purchase library prep and enrichment reagents and index adapters separately.
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Illumina® DNA Prep with Enrichment, (S) Tagmentation (16 Samples)
20025523
Includes reagents for preparing and enriching 16 libraries (16, 1-plex enrichment reactions). Purchase enrichment probe panel, Illumina Purification Beads and index adapters separately.
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Illumina® DNA Prep with Enrichment, (S) Tagmentation (96 Samples)
20025524
Includes reagents for preparing and enriching 96 libraries (eight, 12-plex enrichment reactions). Purchase enrichment probe panel, Illumina Purification Beads and index adapters separately.
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Illumina® DNA Prep, (S) Tagmentation (16 Samples)
20025519
Includes reagents for preparing 16 libraries. No enrichment reagents are included. Purchase enrichment probe panel, Illumina Purification Beads and index adapters separately. Enrichment reagents are only orderable with library prep reagents (Illumina DNA Prep with Enrichment, (S) Tagmentation (16 samples)).
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Illumina® DNA Prep, (S) Tagmentation (96 Samples)
20025520
Includes reagents for preparing 96 libraries. No enrichment reagents are included. Purchase enrichment probe panel, Illumina Purification Beads and index adapters separately. Enrichment reagents are only orderable with library prep reagents (Illumina DNA Prep with Enrichment, (S) Tagmentation (96 samples)).
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IDT® for Illumina® DNA/RNA UD Indexes Set A, Tagmentation (96 Indexes, 96 Samples)
20027213
Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.
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IDT® for Illumina® DNA/RNA UD Indexes Set B, Tagmentation (96 Indexes, 96 Samples)
20027214
Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.
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IDT® for Illumina Nextera DNA Unique Dual Indexes Set C (96 Indexes, 96 Samples)
20027215
IDT for Illumina- Nextera UD Indexes- Set C contains 96, 10 bp unique indexes sufficient for 96 samples. Library prep, enrichment, and enrichment probe panel reagents need to be ordered separately.
IDT® for Illumina Nextera DNA Unique Dual Indexes Set D (96 Indexes, 96 Samples)
20027216
IDT for Illumina- Nextera UD Indexes- Set D contains 96, 10 bp unique indexes sufficient for 96 samples. Library prep, enrichment, and enrichment probe panel reagents need to be ordered separately.
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1. Pua CJ, Bhalshankar J, Miao K, et al. Development of a comprehensive sequencing assay for inherited cardiac condition genes. J Cardiovasc Trans Res. 2016;9:3.
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