Searching journal content for articles similar to Adey and Shendure 22 (6): 1139.

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  1. ...using a DNA polymerase from the 3′ end of the strand that was not subjected to strand transfer then copies the 9-bp overlap region and the ME sequence, terminating at the end of the adapter. In standard tagmentation-based library preparation, this is the reason for the initial extension step in the PCR...
  2. ....0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.References ↵Adey A, Shendure J. 2012. Ultra-low-input, tagmentation-based whole- bisulfite sequencing. Genome Res 22: 1139–1143. ↵Akalin A, Kormaksson M, Li S, Garrett-Bakelman FE, Figueroa ME, Melnick A, Mason CE. 2012. methyl...
  3. ...) to identify putative CREs that have evolved from TE-derived sequences. We then combine these TE-CRE annotations with analyses of the temporal dynamics of TE activity, analyses of gene coexpression, and massive parallel reporter assays. Our results support a link between WGD and TE-CRE evolution and support...
  4. ...Evidence for selfing in a vertebrate from whole- sequencing Astrid Böhne1, Zeynep Oğuzhan1, Ioannis Chrysostomakis1, Simon Vitt2, Denis Meuthen2,3, Sebastian Martin1, Sandra Kukowka1 and Timo Thünken2 1Leibniz Institute for the Analysis of Biodiversity Change LIB, Museum Koenig Bonn, 53113 Bonn...
  5. ...as a major contributing caller to reach final consensus calls by The Cancer Genome Atlas (TCGA) PanCanAtlas project (Ellrott et al. 2018), across approximately 13,000 tumor samples, and the International Cancer Genome Consortium Pan-Cancer Analysis of Whole Genomes (ICGC-PCAWG) initiative (The ICGC/TCGA Pan...
  6. ...Whole- long-read sequencing downsampling and its effect on variant-calling precision and recall William T. Harvey1, Peter Ebert2,3,4, Jana Ebler2,4, Peter A. Audano5, Katherine M. Munson1, Kendra Hoekzema1, David Porubsky1, Christine R. Beck5,6, Tobias Marschall2,4, Kiran Garimella7 and Evan E...
  7. ...Identifying crossovers and shared genetic material in whole sequencing data from families Kelley Paskov1, Brianna Chrisman2, Nathaniel Stockham3, Peter Yigitcan Washington2, Kaitlyn Dunlap1,4, Jae-Yoon Jung1,4 and Dennis P. Wall1,4 1Department of Biomedical Data Science, Stanford University...
  8. ...Haplotype and population structure inference using neural networks in whole- sequencing data Jonas Meisner and Anders Albrechtsen Department of Biology, Bioinformatics Center, University of Copenhagen, DK-2200 Copenhagen, Denmark Corresponding author: jonas...
  9. ...Consortium (ICGC) (Zhang et al. 2019), and the Pan-Cancer Analysis of Whole Genomes (PCAWG) project (The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020) to characterize thousands of cancers across dozens of cancer types. Building on these population-scale efforts, the Catalogue Of Somatic...
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  10. ...several duplicated chromosomes, contradicting current paradigms that asymmetrical evolution is specific to allopolyploids. Altogether, our results offer novel insights into evolutionary dynamics following ancient polyploidizations in vertebrates.Since the first teleost fish sequence was published in 2002...
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