Geoffrey B. Nilsen

发表

Accurate whole genome sequencing and haplotyping from10-20 human cells

Jessica C. Ebert, Madeleine P. Ball, B. Peters, 2012, Nature.

This PDF file includes: Materials and Methods

Robert B. Hartlage, W. C. Banyai, Jessica C. Ebert, 2009 .

A public resource facilitating clinical use of genomes

Euan A Ashley, Jong Bhak, Leonid Peshkin, 2012, Proceedings of the National Academy of Sciences.

Type 2 Diabetes Risk Alleles Demonstrate Extreme Directional Differentiation among Human Populations, Compared to Other Diseases

Alexander A. Morgan, Rong Chen, Atul J. Butte, 2012, PLoS genetics.

Whole-Genome Patterns of Common DNA Variation in Three Human Populations

Geoffrey B. Nilsen, D. Cox, E. Eskin, 2005, Science.

Hinds , in Three Human Populations Whole-Genome Patterns of Common DNA Variation

Eran Halperin, Eleazar Eskin, Kelly A. Frazer, 2008 .

A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

Eleazar Eskin, Molly A. Bogue, Kelly A. Frazer, 2007, Nature.

A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and 77 78 79 80 81 82 Ovarian Cancer Genes in More Than 1000 Patients

Yuya Kobayashi, James M Ford, Stephen E Lincoln, 2015 .

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers.

B. Peters, Geoffrey B. Nilsen, P. Ng, 2014, Cancer research.

Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads

Jessica C. Ebert, PAOLO CARNEVALI, JONATHAN BACCASH, 2012, J. Comput. Biol..

A public resource facilitating clinical use of genomes

Shawn M. Douglas, Jason R. Bobe, W. Chung, 2012, Proceedings of the National Academy of Sciences.

INAUGURAL ARTICLE by a Recently Elected Academy Member:A public resource facilitating clinical use of genomes

Shawn M. Douglas, Jason R. Bobe, W. Chung, 2012 .

A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients.

Geoffrey B. Nilsen, S. Lincoln, K. Jacobs, 2015, The Journal of molecular diagnostics : JMD.

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

Jessica C. Ebert, B. Peters, B. Kermani, 2010, Science.

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers.

B. Peters, Geoffrey B. Nilsen, P. Ng, 2014, Cancer research.