TestEasy
Xpert® MRSA/SA SSTI（包括与我们的合作健康专家进行咨询）
Xpert® MRSA/SA SSTI（包括与我们的合作健康专家进行咨询）
无法加载取货服务可用情况
注意：需要医生处方
请致电我们（+1 450-688-8377 分机 2209）与医生联系。
价格包括咨询和手术
- 包含与我们的合作健康专家的咨询（价值 150 美元）
- 收到样品后当天即可获得结果
- 与公共部门相比，效果更快
- 包含保险索赔收据
Xpert® MRSA/SA SSTI 是一种快速、按需检测的检测方法，可在约一小时内从皮肤和软组织拭子中检测出 MRSA 和 SA。Xpert MRSA/SA SSTI 是目前最全面的金黄色葡萄球菌检测方法：涵盖金黄色葡萄球菌、MRSA 和 mecA 等目标菌种。可识别推定阳性的“空盒”菌株，从而正确归类为 SA 敏感菌株。GeneXpert® 系统无与伦比的自动化功能可减少手动操作时间并提高实验室效率。
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.