微生物多样性测序三代全长扩增子5R 16S rRNA微生物多样性绝对定量 Spike-in宏基因组测序三代宏基因组宏基因组Binning分析宏基因组抗性基因分析宏基因组元素循环分析高宿主污染去除宏基因组项目宏转录组差异表达测序环境宏病毒组测序医学宏病毒组测序高通量16S rDNA菌种鉴定三代DNA宏病毒组MIG-seq肠道宏基因组绝对定量多营养级扩增子扩增子双因素分析动植物基因组Denovo测序细菌基因组测序项目真菌基因组测序项目病毒基因组测序项目简化基因组遗传图谱eQTL简化基因组GWAS测序BSA混池测序基因组SSR开发基因组重测序真核有参转录组测序真核无参转录组测序原核链特异性转录组测序全长转录组(有参_无参)测序LncRNA测序Small RNA测序mGWASMeta-Barcoding(eDNA)技术研究种质资源数字化解决方案转座子插入测序(Tn-seq)PlantArray植物生理组平台染色体级别基因组组装Hi-C建库叶绿体、线粒体基因组测序定制生信分析服务器数据库开发构建服务高通量土壤生物检测Astral蛋白质组学植物单细胞核转录组动物单细胞核转录组动物单细胞转录组单菌株单细菌转录组人肠道单细菌转录组单细胞转录组(SMART)测序靶向代谢组分析非靶向代谢组分析ATAC-seqChip-seqRip-seq全基因组甲基化分析扩增子引物列表资料下载送样指南客户文章列表
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产品简介

宏基因组Binning的方法,可以在自然环境样本中有效区分每个菌株基因组信息。Binning即是从微生物群体序列中将不同个体的序列(readscontigs)分离开的过程。主要用于微生物组的两方面应用:关联分析和单菌组装。



分析流程

宏基因组binning.png



技术参数


实验策略

测序量

项目周期

400bp左右小片段文库

≧30G raw data

70个工作日



技术特色

  • 不依赖于微生物的分离培养,环境微生物单菌基因组(框架图)研究的一种新的途径和高性价比策略;

  • 可以得到环境中丰度较低的宏基因组,为研究低丰度微生物提供了途径;

  • 引入了宏观生态的研究理念,对环境中微生物菌群的多样性、功能活性等宏观特征进行研究,可以更准确地反应出微生物生存的真实状态;

  • 11项目服务,直接对接生信分析师,没有中间环节,沟通更高效;

  • 多组学关联分析,可关联代谢组等研究结果,全方面深化研究。


送样要求


样品类型

样品浓度样品总量

取样材料或者环境样本DNA

30ng/ul1ug



分析示例


宏基因组binning.png




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