Showing results (131-140 of 396) with videos related to
Sort By:
Pageof 40
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2019
Defining the core essential genome of Pseudomonas aeruginosaBradley E Poulsen, Rui Yang, Anne E Clatworthy, et al.Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.Proceedings of the National Academy of Sciences of the United States of America|January 6, 2011
MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13Vijay G Sankaran, Tobias F Menne, Danilo Šćepanović, et al.Nature Methods|December 2, 2008
High-resolution mapping of copy-number alterations with massively parallel sequencingDerek Y Chiang, Gad Getz, David B Jaffe, et al.Nature|April 9, 2025
Spatial multi-omics reveals cell-type-specific nuclear compartmentsYodai Takei, Yujing Yang, Jonathan White, et al.Nature Genetics|November 26, 2024
ChIP-DIP maps binding of hundreds of proteins to DNA simultaneously and identifies diverse gene regulatory elementsAndrew A Perez, Isabel N Goronzy, Mario R Blanco, et al.Nature Biotechnology|August 24, 2021
Single-cell measurement of higher-order 3D genome organization with scSPRITEMary V Arrastia, Joanna W Jachowicz, Noah Ollikainen, et al.Nature|January 7, 2014
Discovery and saturation analysis of cancer genes across 21 tumour typesMichael S Lawrence, Petar Stojanov, Craig H Mermel, et al.Nature Methods|December 17, 2008
Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencingChad Nusbaum, Toshiro K Ohsumi, James Gomez, et al.European Journal of Human Genetics : EJHG|April 13, 2017
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panelMario Mitt, Mart Kals, Kalle Pärn, et al.Pageof 40