Daniel J. Turner

A large genome center's improvements to the Illumina sequencing system.

Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes.

Detection of the BRAF V600E mutation in melanocytic lesions using the ligase detection reaction.

Abridged 5S rDNA units in sea beet (Beta vulgaris subsp. maritima).

Harnessing asymmetrical substrate recognition by thermostable EndoV to achieve balanced linear amplification in multiplexed SNP typing.

Assaying chromosomal inversions by single-molecule haplotyping.

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y.

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.

Long-range, high-throughput haplotype determination via haplotype-fusion PCR and ligation haplotyping.

A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis.

Next-generation sequencing of vertebrate experimental organisms.

Improved protocols for the illumina genome analyzer sequencing system.

TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages.

A simple method for directional transcriptome sequencing using Illumina technology.

Simultaneous assay of every Salmonella Typhi gene using one million transposon mutants.

High-throughput haplotype determination over long distances by haplotype fusion PCR and ligation haplotyping.

FRT-seq: amplification-free, strand-specific transcriptome sequencing.

Target-enrichment strategies for next-generation sequencing.

Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.

CpG islands influence chromatin structure via the CpG-binding protein Cfp1.

iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution.

Orphan CpG islands identify numerous conserved promoters in the mammalian genome.

Whole genome sequencing highlights genetic changes associated with laboratory domestication of C. elegans.

EpiChIP: gene-by-gene quantification of epigenetic modification levels.

CEP152 is a genome maintenance protein disrupted in Seckel syndrome.

Toward clinical proteomics on a next-generation sequencing platform.

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.

High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome.

The GENCODE exome: sequencing the complete human exome.

Amplification-free library preparation for paired-end Illumina sequencing.

96-plex molecular barcoding for the Illumina Genome Analyzer.

High altitude adaptation in Daghestani populations from the Caucasus.

Mobilization of giant piggyBac transposons in the mouse genome.

A barcode screen for epigenetic regulators reveals a role for the NuB4/HAT-B histone acetyltransferase complex in histone turnover.

Low-bias, strand-specific transcriptome Illumina sequencing by on-flowcell reverse transcription (FRT-seq).

Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing data.

Optimizing Illumina Next-Generation Sequencing library preparation for extremely AT-biased genomes.

Behaviour and target site selection of the conjugative transposon Tn916 in two different strains of toxigenic Clostridium difficile.

High-throughput decoding of antitrypanosomal drug efficacy and resistance.