Limitations of mRNA amplification from small-size cell samples

BMC Genomics

Volumn 6, Issue , 2005, Pages

  Nygaard, Vigdis ^a   Holden, Marit ^b   Loland, Anders ^b   Langaas, Mette ^c   Myklebost, Ola ^a   Hovig, Eivind ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b NORWEGIAN COMPUTING CENTER   (Norway)

^c NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; COMPLEMENTARY DNA; PRIMER DNA; RNA;

ANALYSIS OF VARIANCE; ARTICLE; CELL LINE; CONTROLLED STUDY; CORRELATION COEFFICIENT; CYTOLOGY; GENE EXPRESSION PROFILING; HUMAN; HUMAN CELL; METHODOLOGY; NUCLEIC ACID AMPLIFICATION; RELIABILITY; RNA TRANSCRIPTION; SAMPLE SIZE; SENSITIVITY AND SPECIFICITY; CHEMISTRY; DNA MICROARRAY; GENE EXPRESSION REGULATION; GENE LIBRARY; GENETIC PROCEDURES; HELA CELL; METABOLISM; NUCLEIC ACID HYBRIDIZATION; NUCLEOTIDE SEQUENCE; REPRODUCIBILITY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; STATISTICAL MODEL;

ANALYSIS OF VARIANCE; CONSERVED SEQUENCE; DNA PRIMERS; DNA, COMPLEMENTARY; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENE EXPRESSION REGULATION, NEOPLASTIC; GENE LIBRARY; GENETIC TECHNIQUES; HELA CELLS; HUMANS; MODELS, STATISTICAL; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; REPRODUCIBILITY OF RESULTS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA; RNA, MESSENGER; RNA, NEOPLASM;

EID: 27744504822     PISSN: 14712164     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-6-147     Document Type: Article

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