快速生物二代测试服务和产品

  • 让我们帮助您快速获取并理解您得到的大量二代测序数据,以获取有价值的结果。
  • 我们专有的快速验证试剂盒将会使研究人员能够根据二代测序结果快速识别和验证生物靶点功能。
  • 利用二代测序来辅助您在各种疾病诊断和精准治疗做出更准确的判断。
  • 你的生命密码是由DNA序列组成!我们的DNA测试可帮助您设计从健身到营养各个方面的全方位个性化健康指导计划。
我们服务和产品能帮助您!
快速生物公司可以帮助研究人员,科学家和医生利用二代测序能够在更短的时间内获得更有见地的结果。我们公司的主要服务领域包括:
  • 大数据指导下的快速发掘,它提供了二代测序服务和相关的先进生物信息学解决方案,帮助研究人员快速的从大量的基因组数据中得到新发现。
  • 我们的新型和专有快速验证试剂合将使研究人员能够从二代测序结果中快速识别和验证生物靶点的功能。
  • 快速诊断可以让医生利用二代测序在各种疾病诊断和精准治疗做出更准确的判断。
  • 我们的快速指导DNA测试可帮助您设计从健身到营养各个方面的全方位个性化健康指导计划。
快速生物公司为我们提供出色的RNA-seq和其他二代测序服务!
"快速生物公司的服务和技术支持对我们的研究取得成功起到了重要作用,从样品制备到结果交付,此外,周转时间一直比预计的要短,他们对于任何问题回应迅速,任何疑虑都很快得到解决我们对快速生物公司提供的服务非常满意,并计划在可预见的将来再次使用他们的服务!"
- 美国南加州大学Keck医学院助理教授Stefano Da Sacco博士

快速生物已完成的超过200个二代测序项目,并且确保所有的客户100%满意!

自2016年以来,我们帮助世界各地的研究人员完成了他们的二代测序项目,包括RNA-seq,ATAC-seq,ChIP-seq,WGS和WES。

我们拥有最新的Illumina 测序仪

Illumina NovaSeq 6000
HiSeq X Ten
HiSeq 4000
NextSeq 500
MiSeq
Ion Proton

常见问题

  • What is the turn-around time for each of these services?
    In general, the projects of less than 20 samples are completed in between 3 and 4 weeks after we received your samples. Data analysis will need another 1 week. For a big project of more than 20 samples, our turn-around time will be within four weeks and data analysis needs another 1-2 weeks.
  • Will you provide the data analysis service?
    We do provide the comprehensive data analysis for all projects. We have a very strong bioinformatics team which has build up very robust data analysis pipeline of RNA-seq, Whole Exome-Seq, Whole Genome Seq, miRNA-seq, Chip-seq, ATAC-seq, and Methyl-seq. We also provide customized data analysis service based on your request and provide publication quality figure for your project.
  • How can I know the quality of your NGS service?
    We will perform very strict quality control at every step from sample preparation to data analysis. For wet lab part, we will check RNA/DNA sample concentration using Nanodrop and integrity using Bioanalyzer/Tapestation. Then after library construction, we will check the concentration of the library using Qubit and size of the library using Bioanalyzer/Tapestation. For data analysis part, we will check the quality of the raw FASTQ file, remove adaptor and perform quality trimming if necessary. Then we will provide the detailed alignment statistics including mappability, reads distribution in rRNA, intron, exon and intergenic region for RNA_seq. Exome coverage and duplication level will be provided for exome seq. All quality control documents will be sent to our customer. We know the good quality control is the key to a successful project.
  • How many reads (coverage) should I use for my experiment?
    It depends on the goal of your experiment. For gene expression analysis of RNA sequencing, we will recommend 1X 50bp 20M reads. For splicing and gene fusion analysis of RNA sequencing, we will recommend 2X150bp 50M reads. For germline SNV detection of whole exome sequencing, we will recommend 2X150bp 40M reads. For somatic SNV detection of whole exome sequencing, we will recommend 2X150bp 80M reads. For Chip seq and miRNA seq, we will recommend 1X 50bp 20M reads.
  • What is the difference between single reads and paired-end reads?

    In single reads, only one end of the nucleic acid fragments is sequenced. In paired-end reads, the nucleic acid fragments are first sequenced from one end, and then from the other end. This allows generation of high quality, alignable sequence data. Depending on the application, paired-end reads usually do not overlap. Paired-end reads can be used to estimate the fragment size and the duplication level of the library.  In addition, paired-end sequencing allows detection of genomic rearrangements and repetitive sequence elements, as well as gene fusions and novel transcripts.  

您们想要在更短的时间内获得,

解释和验证二代测序结果吗?

今天就联系我们来询价。我们的二代测序专家乐意为您提供帮助!