Challenges with using Primer IDs to improve accuracy of next generation sequencing

PLoS ONE

Volumn 10, Issue 3, 2015, Pages

  Brodin, Johanna ^a   Hedskog, Charlotte ^a   Heddini, Alexander ^a   Benard, Emmanuel ^b   Neher, Richard A ^b   Mild, Mattias ^a,c   Albert, Jan ^a,d  

^a KAROLINSKA INSTITUTE   (Sweden)

^b MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

^c Swedish Institute for Communicable Disease Control   (Sweden)

^d KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; PRIMER DNA;

ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; DNA DEGRADATION; DNA SYNTHESIS; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS INFECTED PATIENT; MEASUREMENT ACCURACY; NEXT GENERATION SEQUENCING; POLYMERASE CHAIN REACTION; PRIMER ID; PROCESS TECHNOLOGY; PYROSEQUENCING; ULTRA DEEP PYROSEQUENCING; GENETICS; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PROCEDURES; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; STANDARDS;

HUMAN IMMUNODEFICIENCY VIRUS 1; RNA VIRUSES;

BASE SEQUENCE; DNA PRIMERS; HIV-1; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 84929157239     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0119123     Document Type: Article

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