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Kevin L. Gunderson

Researcher at Illumina

Publications -  125
Citations -  19532

Kevin L. Gunderson is an academic researcher from Illumina. The author has contributed to research in topics: Nucleic acid & Genome. The author has an hindex of 45, co-authored 125 publications receiving 18276 citations. Previous affiliations of Kevin L. Gunderson include Affymetrix.

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Book ChapterDOI

Whole-genome Genotyping

TL;DR: An array-based whole-genome genotyping (WGG) assay using the BeadChip platform that effectively enables unlimited multiplexing and unconstrained single nucleotide polymorphism (SNP) selection and automation process increases assay robustness and throughput greatly while enabling laboratory information management system control of sample tracking.
Patent

Use of microfluidic systems in the detection of target analytes using microsphere arrays

TL;DR: In this article, the authors describe methods and apparatus for conducting analyses, particularly microfluidic devices for the detection of target analytes, which relates generally to methods and devices for conducting analysis.
Journal ArticleDOI

Mutation Detection by Ligation to Complete n-mer DNA Arrays

TL;DR: A new approach to comparative nucleic acid sequence analysis is described that uses the ligation of DNA targets to high-density arrays containing complete sets of covalently attached oligonucleotides of length eight and nine to demonstrate that complete n-mer arrays can correctly verify known sequences and determine the presence of sequence differences relative to a reference.
Journal ArticleDOI

Subangstrom single-molecule measurements of motor proteins using a nanopore.

TL;DR: Ion current modulation through the protein nanopore MspA is used to observe translocation of helicase Hel308 on DNA with up to ∼40 pm sensitivity, applicable to any protein that translocates on DNA or RNA.
Patent

Nucleic acid sequencing system and method

TL;DR: In this paper, a technique for sequencing nucleic acids in an automated or semi-automated manner is disclosed, in which sample arrays of a multitude of nucleic acid sites are processed in multiple cycles to add nucleotides to the material to be sequenced, detect the nucleotide added to sites, and to de-block the added nucleotide of blocking agents and tags used to identify the last added nucleotide. Quality control routines are run during sequencing to determine quality of samples, and quality of the data collected.