Genomapp. Healthy Ethics.
揭示你的基因组。分析来自 23andMe、Ancestry 等的 DNA 原始数据。
应用信息
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应用描述
Android应用分析和审查：Genomapp. Healthy Ethics.，由RF Developments开发。在健康与健身类别中列出。当前版本为9.0.0，在 11/03/2025 上更新。根据用户在Google Play上的评论：Genomapp. Healthy Ethics.。超过113 千的安装。 Genomapp. Healthy Ethics.目前有890评论，平均评分为4.7星
Genomapp 通过将 DNA 与可靠的科学来源联系起来，帮助您发现 DNA 中的信息。我们的应用程序分析直接面向消费者的基因测试，并以简单的方式呈现结果。你做过DNA测试吗？你知道你的基因组有很多话要说吗？想更多地了解您的 DNA 吗？这比你想象的要容易。
如果您的 DNA 由 DTC 基因检测提供商（例如 23andMe、AncestryDNA、FamilyTreeDNA (FTDNA)、MyHeritage、Genes for Good、Living DNA 或 Geno 2.0）进行了检测，您将可以访问包含您的遗传数据（原始数据）的文件文件）。当您使用 Genomapp 处理此文件时，我们的应用程序会将您输入的 DNA 与条件的分类列表进行匹配。
*** 准备开始？
Genomapp 有演示模式。如果您想尝试该应用程序或了解它的工作原理，您可以访问它并测试该应用程序的全功能版本。
*** Genomapp 提供什么？
Genomapp 免费提供 3 份报告，付款后将提供 3 份报告。
* 复杂疾病（与多因素病症相关的标志物，是多种遗传和环境因素相互作用的结果。）
* 遗传性疾病（与由一种基因突变引起的疾病相关的标记）
* 药理学反应（药物标记物关联）
* 特征（由基因表达和/或受环境影响的特征或属性）
* 可观察到的迹象（与身体问题相关的标记或一个人经历的迹象）
* 血型（与人类血型系统抗原多样性相关的标记）
*** 不是诊断性的
请注意，Genomapp 不用于诊断用途，它不提供医疗建议，也不能替代它。如果您有任何疑问，请咨询您的医疗保健专业人士。
*** 隐私
保护您的隐私是 Genomapp 的首要关注点。
在 Genomapp，我们为人民服务，我们不与第三方共享基因数据，也不利用每个人独特的基因进行交易。
您的数据保留在您的设备中，不会存储或上传到我们的服务器。
*** 认证
该应用程序已经过 mHealth.cat Office（TIC Salut 社会基金会）的审核。这意味着内容的质量及其所包含的功能的实用性已经过评估，并且满足质量和可靠性要求。
*** 我们的数据库
Genomapp 的搜索引擎允许您搜索我们包含超过 9500 个条件、12400 个基因和 180000 个标记的数据库。我们拥有来自官方科学来源的最全面的疾病清单，包括乳腺癌、阿尔茨海默氏症和帕金森氏症。我们还有 BRCA1/2、PTEN 和 P53 等抑癌基因标记。
*** 容易明白
Genomapp 以友好且易于理解的方式显示您的 DNA 标记信息。将您的个性化基因报告导出为 PDF 并随身携带。
*** 您的 DNA 测试提供商不在我们的名单上？
我们不断增加对新 DNA 测试提供商的支持。除了来自最受欢迎的 DTC 基因检测公司（例如 23andMe 或 AncestryDNA）的文件外，Genomapp 还支持 VCF 格式的遗传数据文件和具有特定方案的文件。目前，WES/WGS 中的 VCF 文件与 Genomapp 不兼容。
立即尝试 Genomapp！
我们目前正在提供9.0.0版本。这是我们最新，最优化的版本。它适用于许多不同的设备。从Google Play商店或我们托管的其他版本中免费下载Apk。此外，您可以在不注册的情况下下载且无需登录。
我们拥有超过2000+的Samsung, Xiaomi, Huawei, Oppo, Vivo, Motorola, LG, Google, OnePlus, Sony, Tablet ...设备，并提供了许多选项，您可以轻松选择适合您设备的游戏或软件。
如果在Google App Store上有任何国家限制或设备侧面的任何限制，它可能会派上用场。
什么是新的
New data, better insights! The 2025 Genomapp update is now available. It includes:
- BRCA1 and BRCA2 genes: Over 1000 new markers related to these genes, which are associated with breast and ovarian cancer.
- CFTR gene: 362 new markers added. Mutations in this gene are the leading cause of cystic fibrosis.
- APOE, PSEN1, and PSEN2 genes: 57 new markers related to Alzheimer's disease.
Download the new app and discover what's new!
- BRCA1 and BRCA2 genes: Over 1000 new markers related to these genes, which are associated with breast and ovarian cancer.
- CFTR gene: 362 new markers added. Mutations in this gene are the leading cause of cystic fibrosis.
- APOE, PSEN1, and PSEN2 genes: 57 new markers related to Alzheimer's disease.
Download the new app and discover what's new!
最近的评论
Luana Marquez
As a free app, it's great. But I decided to buy the full thing and was very frustrated. The information is very misleading and lack researches. Basing your whole result in a single research will just lead ppl into anxiety. In the end you have to check all the information there again, by yourself. Which completely loses the point of paying for the product.
Pat Cabrol
Best raw data app there is. I bought the upgrade and have never had any regrets. Great app. Easy to upload raw data and a ton of information. You are able to search the web directly from the reports. I don't understand why this app does not get more press. It is, imho, the only raw data analyzer to use. Thank you to the developers!
Melinda Chandler
The app is very informative and I enjoy learning more about my DNA and genetic markers. However, I cannot recommend downloading the "multifile" feature as it takes so much of a phone's cpu to run that it caused my phone to get really hot/overheat and my display to go black. I couldn't exit the app or do anything other than a hard reset to shut my phone down so it would cool off.
Deborah Noel
Not worth the money... Unless there's more data to come? The info about drugs only scratches the surface and is USA focused. Very little about antibiotics, but lots of opiods. The layout *is* confusing, as someone else says. A note about conflicting signs would be useful to ease people's minds. The frequent alerts re this Not being a diagnostic tool are great, but people are idiots! Add a compulsory learning screen first, maybe? Otherwise, Signs and Traits are v good.
A Google user
Vague descriptions of the genes. Also, some are placed in areas that are confusing...such as medications placed under abnormal response, but show a normal resonse. (?) That doesn't apply to all of them, but it would be nice if it was better laid out.
Mo0nstone Girl
Having uploaded files for myself, husband, daughter and my father I can say the information is consistent. I've always known I have many many health issues, and this app has backed up my belief and I feel alot more comfortable with trusting my instinct. In context, I have 24 different things listed under complex diseases alone, some I'd already known about. I KNOW it's scary to read all that, but it's information I really really needed to know to get the help I need. Thank you.
Mel Pana
When reviewing content the apps touch screen responsiveness is very low which makes it frustrating to use. I purchased the all reports and I can't even look through the findings.
Meah Puckhaber
*Edit-* Yes i will, thank you! Can someone help me? Everything was fine then i got a notification that there was some sort of collaboration you guys did with another company? And said i didn't need to worry cause my genes were going to carry over. And now i can't see any of my reports, when i try to reupload it ALWAYS says that the file is not supported when it's the updated old file.