TestEasy
Xpert® BCR-ABL Ultra（包括与我们的合作伙伴健康专家的咨询）
Xpert® BCR-ABL Ultra（包括与我们的合作伙伴健康专家的咨询）
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 BCR-ABL Ultra 是一款针对 BCR-ABL 主要断点 (p210) 转录本的定量检测，可提供高灵敏度且按需的分子检测结果。Xpert BCR-ABL Ultra 基于创新的 GeneXpert® 技术，在一个全自动卡盒中自动完成整个检测流程，包括 RNA 提取、逆转录以及 BCR-ABL 靶基因和 ABL 参考基因的全嵌套实时 PCR。
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.