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Human Mutation|December 3, 2021
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactylyMarilena Melas, Esko A Kautto, Samuel J Franklin, et al.Nature Methods|August 12, 2009
BreakDancer: an algorithm for high-resolution mapping of genomic structural variationKen Chen, John W Wallis, Michael D McLellan, et al.Cell|January 22, 2019
Characterizing the Major Structural Variant Alleles of the Human GenomePeter A Audano, Arvis Sulovari, Tina A Graves-Lindsay, et al.Nature|January 15, 2010
Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene contentJennifer F Hughes, Helen Skaletsky, Tatyana Pyntikova, et al.Experimental Hematology|August 2, 2017
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomesJin Zhang, Malachi Griffith, Christopher A Miller, et al.Genes, Chromosomes & Cancer|May 27, 2021
Gastroblastoma with a novel EWSR1-CTBP1 fusion presenting in adolescenceSelene C Koo, Stephanie LaHaye, Bence P Kovari, et al.Cell Systems|December 9, 2015
Optimizing cancer genome sequencing and analysisMalachi Griffith, Christopher A Miller, Obi L Griffith, et al.The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.BMC Genomics|December 5, 2021
Discovery of clinically relevant fusions in pediatric cancerStephanie LaHaye, James R Fitch, Kyle J Voytovich, 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.Pageof 3