全自动化序列比对、变异检测、临床解读,无需生物信息专业背景
Fully automatic sequence alignment, variant detection & clinical interpretation
自研增强BLAST+引擎,比NCBI快10~50倍,支持FASTA批量基因序列比对
Enhanced BLAST+ engine, 10-50x faster than NCBI, batch FASTA supported
自动识别肿瘤、遗传病、罕见病致病位点,生成临床级风险报告
Auto-detect cancer, hereditary & rare disease loci with clinical reports
基于基因分型匹配最优靶向药、免疫药,降低耐药与无效治疗
Match optimal drugs based on genotype to reduce drug resistance
致瘤风险、基因编辑脱靶、核型异常检测,满足临床申报标准
Tumorigenicity & off-target detection for clinical stem cell standards
整合人类参考基因组、疾病数据库、药物基因组、干细胞多组学数据,实时更新
Integrate reference genome, disease, pharmacogenomics & stem cell data
GRCh37 / GRCh38 完整版注释
ClinVar、COSMIC、OMIM 权威整合
FDA / NMPA 靶向药靶点数据库
临床级干细胞基因安全标准库
支持医院内网、本地服务器、私有云独立部署,数据不出院,符合医疗隐私合规
Support intranet & local server deployment, fully compliant with medical privacy
完全本地化运行,不依赖外网,基因数据100%自主可控
Local running without internet, 100% data control
符合HIPAA与国内健康医疗数据安全规范
实验室、医生、管理员分级权限,安全审计
对接LIS/HIS/检验系统,一键自动化分析