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Volumn 2, Issue 2, 2007, Pages
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The use of coded PCR primers enables high-throughput sequencing of multiple homolog amplification products by 454 parallel sequencing
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Author keywords
[No Author keywords available]
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Indexed keywords
CYTOSINE;
DINUCLEOTIDE;
DNA;
NUCLEOTIDE;
THYMINE;
MITOCHONDRIAL DNA;
PRIMER DNA;
ARTICLE;
CONTROLLED STUDY;
DNA DETERMINATION;
DNA SEQUENCE;
DNA SYNTHESIS;
GENE ASSIGNMENT;
GENE SEQUENCE;
GENETIC CODE;
HIGH THROUGHPUT SCREENING;
HUMAN;
NONHUMAN;
NUCLEIC ACID AMPLIFICATION;
POLYMERASE CHAIN REACTION;
SEQUENCE ANALYSIS;
SEQUENCE HOMOLOGY;
ANIMAL;
GENE AMPLIFICATION;
GENETICS;
INSTRUMENTATION;
METHODOLOGY;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
SEQUENCE ALIGNMENT;
SPECIES DIFFERENCE;
ANIMALS;
BASE SEQUENCE;
DNA PRIMERS;
DNA, MITOCHONDRIAL;
GENE AMPLIFICATION;
HIGH-THROUGHPUT SCREENING ASSAYS;
HUMANS;
MOLECULAR SEQUENCE DATA;
POLYMERASE CHAIN REACTION;
SEQUENCE ALIGNMENT;
SEQUENCE ANALYSIS, DNA;
SEQUENCE HOMOLOGY, NUCLEIC ACID;
SPECIES SPECIFICITY;
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EID: 34547834963
PISSN: None
EISSN: 19326203
Source Type: Journal
DOI: 10.1371/journal.pone.0000197 Document Type: Article |
Times cited : (428)
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References (7)
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