即使没有平台参与，您也可以通过FastTrack测序服务来享有Illumina测序技术的力量。我们数年来提供高品质服务，具有丰富的咨询和分析能力，能适度调整以满足您的需求。我们成功开展高价值项目的记录，以及我们所提供的经验丰富专家团队，将让边合成边测序技术便利且负担得起。依靠Illumina的FastTrack测序服务组来设计和完成您的项目，其记录时间和费用都是其它任何技术无法匹敌的。


提供的应用:

  • 全基因组测序
  • 候选基因和区域重测序
  • 细菌DNA重测序
  • 数字表达谱
  • 小RNA发现

如果您所感兴趣的应用不在上述列表，请联系我们。我们会与您合作，设计出合适的步骤和过程，以应对您的应用。

FastTrack测序服务组将在整个流程内为您提供帮助:

  • 实验设计的咨询
  • 样品制备和质量控制
  • 簇生成
  • 利用Illumina的Genome Analyzer边合成边测序
  • 数据分析和生物信息学咨询


全基因组测序

FastTrack测序服务借助Illlumian独有的边合成边测序技术和Genome Analyzer IIx的力量，提供了全基因组测序的经济方案。我们目前提供三个全基因组测序包，在多个生物学发现应用中具有行业领先的覆盖度和数据质量。


全基因组测序包

Human whole-genome paired-end sequencing, short and long inserts
This package includes:
  • Consensus sequence built with ELAND using short-insert paired-end reads at minimum 30x average sequence coverage, and 2 kb and 4 kb long-fragment mate-pair reads at minimum 30x average physical coverage
  • Called SNPs, insertion/deletion events and information on larger structural variants using CASAVA
  • Dataset including all reads and quality scores for further downstream analysis
  • Minimum sample input is 20 µg gDNA to create three libraries.
Human whole-genome paired-end sequencing, short inserts
This package includes:
  • Sequence built with ELAND alignment using short-insert paired end reads only (200-400 bp) at minimum 30x average sequence coverage
  • Called SNPs and short insertion/deletion information plus limited information on larger structural variants using CASAVA
  • Dataset including all reads and quality scores for further downstream analysis
  • Minimum sample input of 5 µg gDNA to create one library.
Non-human whole-genome paired-end sequencing
This package is available for researchers resequencing species with known reference sequences. Dependent on the complexity of the genome and the quality of annotation available, the package may include:
  • Consensus sequence, built using short-insert paired-end reads (200-400 bp) with a minimum of 30x average sequence coverage, as well as 2 kb and 4 kb (or longer as necessary) long-insert mate-pair reads at a minimum of 30x average physical coverage
  • Called SNPs and short insertions/deletions using CASAVA
  • Dataset including all reads and quality scores for further downstream analysis
  • Minimum sample input of 20 µg gDNA to create three libraries.


* For research use only.