4.2 Article

No assembly required: Full-length MHC class I allele discovery by PacBio circular consensus sequencing

期刊

HUMAN IMMUNOLOGY
卷 76, 期 12, 页码 891-896

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.humimm.2015.03.022

关键词

MHC class I; Cynomolgus macaques; Single-molecule real-time circular consensus sequencing (SMRT-CCS); PacBio

资金

  1. Defense Threat Reduction Agency under USAMRIID project [3174512]
  2. National Institute of Allergy and Infectious Diseases [HHSN272201100013C]
  3. Research Facilities Improvement Program [RR15459-01, RR020141-01]

向作者/读者索取更多资源

Single-molecule real-time (SMRT) sequencing technology with the Pacific Biosciences (PacBio) RS II platform offers the potential to obtain full-length coding regions (similar to 1100-bp) from MHC class I cDNAs. Despite the relatively high error rate associated with SMRT technology, high quality sequences can be obtained by circular consensus sequencing (CCS) due to the random nature of the error profile. In the present study we first validated the ability of SMRT-CCS to accurately identify class I transcripts in Mauritian-origin cynomolgus macaques (Macaca fascicularis) that have been characterized previously by cloning and Sanger-based sequencing as well as pyrosequencing approaches. We then applied this SMRT-CCS method to characterize 60 novel full-length class I transcript sequences expressed by a cohort of cynomolgus macaques from China. The SMRT-CCS method described here provides a straightforward protocol for characterization of unfragmented single-molecule cDNA transcripts that will potentially revolutionize MHC class I allele discovery in nonhuman primates and other species. Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics.

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