L. Cook

发表

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

M. Daly, G. Marth, E. Lander, 2001, Nature.

Genome Remodeling in a Basal-like Breast Cancer Metastasis and Xenograft

Joshua F. McMichael, James M. Eldred, Benjamin J. Oberkfell, 2010, Nature.

Initial sequencing and analysis of the human genome.

J. V. Moran, V. J. Pollara, D. Haussler, 2001, Nature.

Initial sequencing and comparative analysis of the mouse genome.

Colin N. Dewey, Simon C. Potter, James A. Cuff, 2002 .

Comparative and demographic analysis of orang-utan genomes

Albert J. Vilella, Zhengyuan O. Wang, Matthew W. Hahn, 2011, Nature.

Integrated Genomic Analyses of Ovarian Carcinoma

Benjamin J. Raphael, James M. Eldred, Joshua M. Stuart, 2011, Nature.

DNA sequencing of a cytogenetically normal acute myeloid leukemia genome

Amy E. Hawkins, Brian H. Dunford-Shore, R. Wilson, 2008, Nature.

Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing

Joshua F. McMichael, Christopher A. Miller, Joelle M. Kalicki-Veizer, 2011, Nature.

The Origin and Evolution of Mutations in Acute Myeloid Leukemia

Joshua F. McMichael, Christopher A. Miller, Joelle M. Kalicki-Veizer, 2012, Cell.

Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921))

Ronald W. Davis, J. V. Moran, V. J. Pollara, 2001 .

The prognostic effects of somatic mutations in ER-positive breast cancer

Benjamin J. Ainscough, Katie M. Campbell, Christopher A. Miller, 2017, Nature Communications.

The prognostic effects of somatic mutations in ER-positive breast cancer

Benjamin J. Ainscough, Katie M. Campbell, Christopher A. Miller, 2017, bioRxiv.

DNMT3A mutations in acute myeloid leukemia.

Joshua F. McMichael, Cheryl F. Lichti, R. Wilson, 2010, The New England journal of medicine.

Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression.

P. Cahan, R. Wilson, R. Fulton, 2011, The Journal of clinical investigation.

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

Terrence S. Furey, Sean R. Eddy, Li Ding, 2005, Nature.

Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells.

Christopher A. Miller, Joelle M. Kalicki-Veizer, R. Wilson, 2012, Cell stem cell.

The DNA sequence of human chromosome 7

James M. Eldred, M. Suyama, E. Eichler, 2003, Nature.

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

Supplemental Section S1 – Genome Sequencing and Assembly........................................... 2 Supplemental Section S2 – Indel Assessment with the Neutral Indel Model ................11 Supplemental Section S3 – Great Ape Divergence Estimate via Wgs Read Mapping..11 Supplemental Section S7 –

Albert J. Vilella, Zhengyuan O. Wang, Miriam K. Konkel, 2022 .

DNMT 3 A mutations in acute myeloid leukemia

Joshua F. McMichael, Cheryl F. Lichti, R. Wilson, 2016 .

Supplementary Materials Rationale for Selection an Aml Genome for Sequencing. We Selected a Specific Genome for Study Based on the following Criteria

Amy E. Hawkins, Brian H. Dunford-Shore, R. Wilson, 2022 .

Copy number heterogeneity, large origin tandem repeats, and interspecies recombination in HHV-6A and HHV-6B reference strains

L. Cook, Lauren M. Saunders, Meei-Li W Huang, 2017, bioRxiv.

Tracking the prevalence and emergence of SARS CoV2 variants of concern using a regional genomic surveillance program

Bijal A. Parikh, L. Cook, David Wang, 2023, medRxiv.

Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells.

Christopher A. Miller, Joelle M. Kalicki-Veizer, E. Mardis, 2012, Cell stem cell.