Optimizing illumina next-generation sequencing library preparation for extremely at-biased genomes

BMC Genomics

Volumn 13, Issue 1, 2012, Pages

  Oyola, Samuel O ^a   Otto, Thomas D ^a   Gu, Yong ^a   Maslen, Gareth ^a   Manske, Magnus ^a   Campino, Susana ^a   Turner, Daniel J ^b   MacInnis, Bronwyn ^a   Kwiatkowski, Dominic P ^a   Swerdlow, Harold P ^a   Quail, Michael A ^a  

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b Oxford Nanopore Technologies Ltd   (United Kingdom)

Author keywords

At rich; Clinical isolate; Exponential; Illumina; Isothermal; Library; Linear; Malaria; Next generation sequencing; PCR; PCR free; Plasmodium falciparum; Tetramethyammonium chloride

Indexed keywords

SINGLE STRANDED DNA; BACTERIOPHAGE T7 RNA POLYMERASE; DNA DIRECTED RNA POLYMERASE; VIRUS PROTEIN;

ARTICLE; AT RICH SEQUENCE; CHROMOSOME 11; CONTROLLED STUDY; DNA BASE COMPOSITION; DNA TEMPLATE; GENE AMPLIFICATION; GENE LIBRARY; GENETIC PROCEDURES; GENOME; MYCOBACTERIUM TUBERCULOSIS; NEXT GENERATION SEQUENCING; NONHUMAN; PARASITE ISOLATION; PLASMODIUM FALCIPARUM; POLYMERASE CHAIN REACTION; QUALITY CONTROL; THERMOSTABILITY; GENE LOCUS; GENETICS; HIGH THROUGHPUT SEQUENCING; METABOLISM; METHODOLOGY; REPRODUCIBILITY;

MYCOBACTERIUM TUBERCULOSIS; PLASMODIUM FALCIPARUM;

BASE COMPOSITION; DNA-DIRECTED RNA POLYMERASES; GENE LIBRARY; GENETIC LOCI; GENOME, PROTOZOAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; PLASMODIUM FALCIPARUM; POLYMERASE CHAIN REACTION; REPRODUCIBILITY OF RESULTS; VIRAL PROTEINS;

EID: 84855219212     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-13-1     Document Type: Article

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