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Arxiv|December 19, 2025
ImmunoNX: a robust bioinformatics workflow to support personalized neoantigen vaccine trialsKartik Singhal, Evelyn Schmidt, Susanna Kiwala, et al.Nature|April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversityTing Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.Nature|January 13, 2012
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencingLi Ding, Timothy J Ley, David E Larson, et al.Cell|April 7, 2018
Pathogenic Germline Variants in 10,389 Adult CancersKuan-Lin Huang, R Jay Mashl, Yige Wu, et al.Nature Communications|December 23, 2015
Patterns and functional implications of rare germline variants across 12 cancer typesCharles Lu, Mingchao Xie, Michael C Wendl, et al.The New England Journal of Medicine|November 12, 2010
DNMT3A mutations in acute myeloid leukemiaTimothy J Ley, Li Ding, Matthew J Walter, et al.Cell Reports|September 24, 2013
Endocrine-therapy-resistant ESR1 variants revealed by genomic characterization of breast-cancer-derived xenograftsShunqiang Li, Dong Shen, Jieya Shao, et al.Cell|July 24, 2012
The origin and evolution of mutations in acute myeloid leukemiaJohn S Welch, Timothy J Ley, Daniel C Link, et al.Nature|June 23, 2012
Whole-genome analysis informs breast cancer response to aromatase inhibitionMatthew J Ellis, Li Ding, Dong Shen, et al.The New England Journal of Medicine|August 7, 2009
Recurring mutations found by sequencing an acute myeloid leukemia genomeElaine R Mardis, Li Ding, David J Dooling, et al.Pageof 4