Ebogenes Store
Omega-3 指数（完整测试套件）
Omega-3 指数（完整测试套件）
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Omega-3 指数测试是一项先进的血斑检测，旨在测量您的Omega-3 指数，即红细胞 (RBC) 膜中关键 Omega-3 脂肪酸EPA（二十碳五烯酸）和DHA（二十二碳六烯酸）的百分比。除了这项关键指标外，该测试还能全面分析您血液中所有脂肪酸的含量，包括 Omega-6、反式脂肪、饱和脂肪和单不饱和脂肪。
为什么它很重要：
- 健康 Omega-3指数 的 8%–12% 链接到 最低风险 死于心脏病，而低于 4% 与 最高风险。
- 该测试还评估其他健康指标，包括：
- Omega-6：Omega-3 比率：炎症平衡的关键指标。
- AA：EPA 比率：炎症和心血管健康的关键标志。
- 完整的脂肪酸分解可以洞察你的 总体营养状况 和代谢健康。
您将收到：
- 你的 Omega-3指数 评分来评估长期的 omega-3 状态。
- 详细分析 所有脂肪酸 在您的红细胞膜中，包括：
- Omega-3（EPA、DHA、DPA）
- Omega-6脂肪酸
- 反式脂肪指数
- 单不饱和脂肪和饱和脂肪
- 通过饮食调整或补充来优化 omega-3 水平的易于理解的见解和个性化建议。
好处：
- 准确、可靠地反映您过去的 Omega-3 摄入量 3-4个月。
- 识别脂肪酸失衡，以更好地支持 心脏、大脑和代谢健康。
- 长期的主动工具 健康监测。
掌控您的健康：
通过了解您的脂肪酸状况并优化您的 Omega-3 指数，您可以采取有意义的措施来减少炎症、支持心血管健康并提升整体健康水平。为了获得最佳效果，建议每3-6 个月定期复测一次。
All 6.4 billion letters of your DNA — read, stored, and yours to keep.
Most consumer DNA tests sample a few hundred thousand positions. Whole genome sequencing reads the entire thing at 30× depth, and hands you the files at the end. No subscription required to keep them.
-
30×
average
coverage depth -
6.4B
base pairs
sequenced -
FASTQ
BAM & VCF
files included
How it runs
Kit arrives
Day 0，Saliva collection takes about five minutes. Avoid eating, drinking, or brushing your teeth for thirty minutes beforehand — that's the only preparation required.
Sample ships back
Day 1–2， Prepaid return envelope is included. Saliva samples are stable at room temperature, so there's no cold chain to manage on your end.
DNA extraction and quality check
Week 1，We extract and assess DNA quality before sequencing. If a sample fails QC, we send a replacement kit at no charge rather than sequencing something that won't yield reliable calls.
Sequencing and analysis
Week 2–6，Sequencing, alignment to GRCh38, and variant calling. This is the longest stage and we'd rather state it accurately than quote a number we miss.
Reports and files released
Week 2–6， Your reports and all three file formats become available together. You'll get an email the moment they're ready.
No. Ebogenes whole genome sequencing is offered for research and personal informational use. It is not a diagnostic test, it is not a substitute for clinical genetic testing, and it should not be used to make medical decisions on its own. If a finding concerns you, bring it to a physician or a certified genetic counsellor — that's what the files are for.
Each position in your genome is read approximately thirty times on average. Sequencing makes errors, so reading a position once tells you little; reading it thirty times lets a variant call rest on consensus. 30× is the widely used standard for reliable variant calling — below it, calls get noticeably less dependable.
Our reports flag findings for follow-up; they do not diagnose. A variant of uncertain significance is a flag, not a finding — many are later reclassified as benign. We'd rather tell you plainly that something needs a professional look than dress up an uncertain result as an answer.
Sequencing and storage happen at our Laval, Québec facility. Your data stays in Canada and is subject to Canadian privacy law. We do not sell your genetic data, and we do not share it with insurers, employers, or research programmes without your explicit, separate consent. You can request deletion at any time.
No. Your reports and all three file formats remain accessible without any ongoing payment. Download them and store your own copy if you prefer — that's the point of giving you FASTQ.