TestEasy
运动潜能基因检测
运动潜能基因检测
无法加载取货服务可用情况
1.摘要
你的基因构成在决定你的身体能力和运动表现方面起着至关重要的作用。运动基因分析可以检测与力量、耐力、新陈代谢和受伤风险相关的基因标记，帮助你定制训练计划，优化运动表现。
2. 背景
每位运动员的身体对体力活动的反应都不同。有些人擅长力量型运动，例如举重，而另一些人则更适合跑步或骑行等耐力型运动。这些差异不仅源于训练和饮食，还与遗传因素有关。特定的基因变异会影响身体的肌肉生成、氧气处理以及运动后恢复。
运动基因分析可以识别关键的基因标记，揭示您是否具有某些特质，例如速度、耐力或易受伤。有了这些信息，您就可以定制训练方案，最大限度地发挥您的优势，并最大限度地降低受伤风险。
3.技术概述
- ACTN3 基因：ACTN3 基因被称为“速度基因”，与快肌纤维相关，而快肌纤维对于短跑等爆发性运动至关重要。该基因的变异可以指示您是否在基因上倾向于在力量型或耐力型运动中表现出色。
- PPARGC1A基因：该基因与耐力表现相关，因为它会影响身体在运动过程中对氧气的利用。携带特定变异的个体可能在长跑或骑行等活动中拥有天然优势。
- COL5A1基因：该基因的变异会影响胶原蛋白的生成，从而影响肌腱的强度和柔韧性。了解您的COL5A1状态有助于预防损伤，尤其是在高强度运动中。
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.
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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.