Daniel J. Turner

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 203	2011

Other Publications

Article	Year
A large genome center's improvements to the Illumina sequencing system. Nature methods\| PubMed ID: 19034268	2008
Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes. Nature methods\| PubMed ID: 19287394	2009
Detection of the BRAF V600E mutation in melanocytic lesions using the ligase detection reaction. Journal of cutaneous pathology\| PubMed ID: 15811117	2005
Abridged 5S rDNA units in sea beet (Beta vulgaris subsp. maritima). Genome / National Research Council Canada = GÃ©nome / Conseil national de recherches Canada\| PubMed ID: 15838559	2005
Harnessing asymmetrical substrate recognition by thermostable EndoV to achieve balanced linear amplification in multiplexed SNP typing. Biochemistry and cell biology = Biochimie et biologie cellulaire\| PubMed ID: 16609704	2006
Assaying chromosomal inversions by single-molecule haplotyping. Nature methods\| PubMed ID: 16721377	2006
Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y. Human molecular genetics\| PubMed ID: 17189292	2007
Germline rates of de novo meiotic deletions and duplications causing several genomic disorders. Nature genetics\| PubMed ID: 18059269	2008
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nature genetics\| PubMed ID: 18438408	2008
Long-range, high-throughput haplotype determination via haplotype-fusion PCR and ligation haplotyping. Nucleic acids research\| PubMed ID: 18562465	2008
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis. Nature biotechnology\| PubMed ID: 18612301	2008
Next-generation sequencing of vertebrate experimental organisms. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 19452216	2009
Improved protocols for the illumina genome analyzer sequencing system. Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.]\| PubMed ID: 19582764	2009
TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages. The Journal of clinical endocrinology and metabolism\| PubMed ID: 19773397	2009
A simple method for directional transcriptome sequencing using Illumina technology. Nucleic acids research\| PubMed ID: 19815668	2009
Simultaneous assay of every Salmonella Typhi gene using one million transposon mutants. Genome research\| PubMed ID: 19826075	2009
High-throughput haplotype determination over long distances by haplotype fusion PCR and ligation haplotyping. Nature protocols\| PubMed ID: 20010928	2009
FRT-seq: amplification-free, strand-specific transcriptome sequencing. Nature methods\| PubMed ID: 20081834	2010
Target-enrichment strategies for next-generation sequencing. Nature methods\| PubMed ID: 20111037	2010
Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state. Molecular cell\| PubMed ID: 20188665	2010
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs. Nature genetics\| PubMed ID: 20364136	2010
CpG islands influence chromatin structure via the CpG-binding protein Cfp1. Nature\| PubMed ID: 20393567	2010
iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution. Nature structural & molecular biology\| PubMed ID: 20601959	2010
Orphan CpG islands identify numerous conserved promoters in the mammalian genome. PLoS genetics\| PubMed ID: 20885785	2010
Whole genome sequencing highlights genetic changes associated with laboratory domestication of C. elegans. PloS one\| PubMed ID: 21085631	2010
EpiChIP: gene-by-gene quantification of epigenetic modification levels. Nucleic acids research\| PubMed ID: 21131282	2011
CEP152 is a genome maintenance protein disrupted in Seckel syndrome. Nature genetics\| PubMed ID: 21131973	2011
Toward clinical proteomics on a next-generation sequencing platform. Analytical chemistry\| PubMed ID: 21142014	2011
Retrospective application of transposon-directed insertion site sequencing to a library of signature-tagged mini-Tn5Km2 mutants of Escherichia coli O157:H7 screened in cattle. Journal of bacteriology\| PubMed ID: 21278291	2011
High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome. Genome research\| PubMed ID: 21363968	2011
The GENCODE exome: sequencing the complete human exome. European journal of human genetics : EJHG\| PubMed ID: 21364695	2011
Amplification-free library preparation for paired-end Illumina sequencing. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21431776	2011
96-plex molecular barcoding for the Illumina Genome Analyzer. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21431778	2011
High altitude adaptation in Daghestani populations from the Caucasus. Human genetics\| PubMed ID: 21904933	2012
Mobilization of giant piggyBac transposons in the mouse genome. Nucleic acids research\| PubMed ID: 21948799	2011
A barcode screen for epigenetic regulators reveals a role for the NuB4/HAT-B histone acetyltransferase complex in histone turnover. PLoS genetics\| PubMed ID: 21998594	2011
Low-bias, strand-specific transcriptome Illumina sequencing by on-flowcell reverse transcription (FRT-seq). Nature protocols\| PubMed ID: 22015844	2011
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing data. Human genetics\| PubMed ID: 22057783	2011
Optimizing Illumina Next-Generation Sequencing library preparation for extremely AT-biased genomes. BMC genomics\| PubMed ID: 22214261	2012
Behaviour and target site selection of the conjugative transposon Tn916 in two different strains of toxigenic Clostridium difficile. Applied and environmental microbiology\| PubMed ID: 22267673	2012
High-throughput decoding of antitrypanosomal drug efficacy and resistance. Nature\| PubMed ID: 22278056	2012