Two methods for full-length RNA sequencing for low quantities of cells and single cells

Proceedings of the National Academy of Sciences of the United States of America

Volumn 110, Issue 2, 2013, Pages 594-599

  Pan, Xinghua ^a   Durrett, Russell E ^b   Zhu, Haiying ^a,c   Tanaka, Yoshiaki ^a   Li, Yumei ^a,d   Zi, Xiaoyuan ^a   Marjani, Sadie L ^a   Euskirchen, Ghia ^e   Ma, Chao ^a,f   LaMotte, Robert H ^a   Park, In Hyun ^a   Snyder, Michael P ^e   Mason, Christopher E ^b   Weissman, Sherman M ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WEILL CORNELL MEDICAL COLLEGE   (United States)

^c SECOND MILITARY MEDICAL UNIVERSITY   (China)

^d AFFILIATED HOSPITAL OF JIANGSU UNIVERSITY   (China)

^e STANFORD UNIVERSITY   (United States)

^f INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

Author keywords

Full length mRNA; RNA seq; Single cell analysis; Transcriptome ampli fication

Indexed keywords

COMPLEMENTARY DNA; DNA POLYMERASE; MESSENGER RNA; OLIGODEOXYNUCLEOTIDE; OLIGONUCLEOTIDE;

ARTICLE; ERYTHROLEUKEMIA CELL; GENE AMPLIFICATION; GENE EXPRESSION; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA DEGRADATION; RNA SEQUENCE; SINGLE CELL ANALYSIS;

DNA PRIMERS; GENE EXPRESSION PROFILING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; K562 CELLS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POLYMERASE CHAIN REACTION; RNA, MESSENGER; SINGLE-CELL ANALYSIS;

EID: 84872194966     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1217322109     Document Type: Article

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