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Richard K. Wilson

Researcher at Nationwide Children's Hospital

Publications -  501
Citations -  294778

Richard K. Wilson is an academic researcher from Nationwide Children's Hospital. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 173, co-authored 463 publications receiving 260000 citations. Previous affiliations of Richard K. Wilson include University of Washington & St. Jude Children's Research Hospital.

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Journal ArticleDOI

A physical map of human chromosome 14.

TL;DR: The construction of a tiling path of around 650 clones covering more than 99% of human chromosome 14 indicates that the sequence tag connector approach compares favourably with alternative mapping strategies.
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The construction and analysis of M13 libraries prepared from YAC DNA

TL;DR: It is shown that sequencing at about 1-fold coverage, followed by database comparison (survey sequencing) offers a relatively quick method to determine the nature of previously uncharacterized cosmid or YAC clones.
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Mutational landscape and response are conserved in peripheral blood of AML and MDS patients during decitabine therapy.

TL;DR: Quantitative response evaluation in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDSs) relies on the morphologic quantification of bone marrow blasts, subject to the operator-dependent quality of BM collection and the interobserver variability.
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Theories and Applications for Sequencing Randomly Selected Clones

TL;DR: It is concluded that the map-based approach outperforms random clone sequencing, except early in a project, and that simultaneous use of both strategies can be beneficial if a performance-based estimate for halting random clones is made.
Posted ContentDOI

High-Quality Assembly of an Individual of Yoruban Descent

TL;DR: This work uses PacBio single-molecule, real-time (SMRT) sequencing and BioNano genomic maps to construct the first de novo assembly of NA19240, a Yoruban individual from Africa, and demonstrates that diploid assembly has utility in improving the quality of de noVO human genome assemblies.