Search Results - "DAZA, Riza"

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    Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin by Snyder, Matthew W., Kircher, Martin, Hill, Andrew J., Daza, Riza M., Shendure, Jay

    Published in Cell (14-01-2016)
    “…Nucleosome positioning varies between cell types. By deep sequencing cell-free DNA (cfDNA), isolated from circulating blood plasma, we generated maps of…”
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    Cicero Predicts cis-Regulatory DNA Interactions from Single-Cell Chromatin Accessibility Data by Pliner, Hannah A., Packer, Jonathan S., McFaline-Figueroa, José L., Cusanovich, Darren A., Daza, Riza M., Aghamirzaie, Delasa, Srivatsan, Sanjay, Qiu, Xiaojie, Jackson, Dana, Minkina, Anna, Adey, Andrew C., Steemers, Frank J., Shendure, Jay, Trapnell, Cole

    Published in Molecular cell (06-09-2018)
    “…Linking regulatory DNA elements to their target genes, which may be located hundreds of kilobases away, remains challenging. Here, we introduce Cicero, an…”
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  3. 3

    The cis-regulatory dynamics of embryonic development at single-cell resolution by Cusanovich, Darren A., Reddington, James P., Garfield, David A., Daza, Riza M., Aghamirzaie, Delasa, Marco-Ferreres, Raquel, Pliner, Hannah A., Christiansen, Lena, Qiu, Xiaojie, Steemers, Frank J., Trapnell, Cole, Shendure, Jay, Furlong, Eileen E. M.

    Published in Nature (London) (22-03-2018)
    “…An improved assay for chromatin accessibility at single-cell resolution in Drosophila melanogaster embryos enables identification of developmental-stage- and…”
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    A human cell atlas of fetal gene expression by Cao, Junyue, O'Day, Diana R, Pliner, Hannah A, Kingsley, Paul D, Deng, Mei, Daza, Riza M, Zager, Michael A, Aldinger, Kimberly A, Blecher-Gonen, Ronnie, Zhang, Fan, Spielmann, Malte, Palis, James, Doherty, Dan, Steemers, Frank J, Glass, Ian A, Trapnell, Cole, Shendure, Jay

    “…The gene expression program underlying the specification of human cell types is of fundamental interest. We generated human cell atlases of gene expression and…”
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    Precise genomic deletions using paired prime editing by Choi, Junhong, Chen, Wei, Suiter, Chase C., Lee, Choli, Chardon, Florence M., Yang, Wei, Leith, Anh, Daza, Riza M., Martin, Beth, Shendure, Jay

    Published in Nature biotechnology (01-02-2022)
    “…Current methods to delete genomic sequences are based on clustered regularly interspaced short palindromic repeats (CRISPR)–Cas9 and pairs of single-guide RNAs…”
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    Pluripotent stem cell-derived model of the post-implantation human embryo by Weatherbee, Bailey A. T., Gantner, Carlos W., Iwamoto-Stohl, Lisa K., Daza, Riza M., Hamazaki, Nobuhiko, Shendure, Jay, Zernicka-Goetz, Magdalena

    Published in Nature (London) (19-10-2023)
    “…The human embryo undergoes morphogenetic transformations following implantation into the uterus, but our knowledge of this crucial stage is limited by the…”
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    A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility by Cusanovich, Darren A., Hill, Andrew J., Aghamirzaie, Delasa, Daza, Riza M., Pliner, Hannah A., Berletch, Joel B., Filippova, Galina N., Huang, Xingfan, Christiansen, Lena, DeWitt, William S., Lee, Choli, Regalado, Samuel G., Read, David F., Steemers, Frank J., Disteche, Christine M., Trapnell, Cole, Shendure, Jay

    Published in Cell (23-08-2018)
    “…We applied a combinatorial indexing assay, sci-ATAC-seq, to profile genome-wide chromatin accessibility in ∼100,000 single cells from 13 adult mouse tissues…”
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    Accurate classification of BRCA1 variants with saturation genome editing by Findlay, Gregory M., Daza, Riza M., Martin, Beth, Zhang, Melissa D., Leith, Anh P., Gasperini, Molly, Janizek, Joseph D., Huang, Xingfan, Starita, Lea M., Shendure, Jay

    Published in Nature (London) (01-10-2018)
    “…Variants of uncertain significance fundamentally limit the clinical utility of genetic information. The challenge they pose is epitomized by BRCA1 , a tumour…”
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    Comprehensive single-cell transcriptional profiling of a multicellular organism by Cao, Junyue, Packer, Jonathan S., Ramani, Vijay, Cusanovich, Darren A., Huynh, Chau, Daza, Riza, Qiu, Xiaojie, Lee, Choli, Furlan, Scott N., Steemers, Frank J., Adey, Andrew, Waterston, Robert H., Trapnell, Cole, Shendure, Jay

    “…To resolve cellular heterogeneity, we developed a combinatorial indexing strategy to profile the transcriptomes of single cells or nuclei, termed sci-RNA-seq…”
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    A time-resolved, multi-symbol molecular recorder via sequential genome editing by Choi, Junhong, Chen, Wei, Minkina, Anna, Chardon, Florence M., Suiter, Chase C., Regalado, Samuel G., Domcke, Silvia, Hamazaki, Nobuhiko, Lee, Choli, Martin, Beth, Daza, Riza M., Shendure, Jay

    Published in Nature (London) (04-08-2022)
    “…DNA is naturally well suited to serve as a digital medium for in vivo molecular recording. However, contemporary DNA-based memory devices are constrained in…”
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    Multiplex single-cell profiling of chromatin accessibility by combinatorial cellular indexing by Cusanovich, Darren A., Daza, Riza, Adey, Andrew, Pliner, Hannah A., Christiansen, Lena, Gunderson, Kevin L., Steemers, Frank J., Trapnell, Cole, Shendure, Jay

    “…Technical advances have enabled the collection of genome and transcriptome data sets with single-cell resolution. However, single-cell characterization of the…”
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    Fragment Length of Circulating Tumor DNA by Underhill, Hunter R, Kitzman, Jacob O, Hellwig, Sabine, Welker, Noah C, Daza, Riza, Baker, Daniel N, Gligorich, Keith M, Rostomily, Robert C, Bronner, Mary P, Shendure, Jay

    Published in PLoS genetics (01-07-2016)
    “…Malignant tumors shed DNA into the circulation. The transient half-life of circulating tumor DNA (ctDNA) may afford the opportunity to diagnose, monitor…”
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    Copy-Number Variation and False Positive Prenatal Aneuploidy Screening Results by Snyder, Matthew W, Simmons, LaVone E, Kitzman, Jacob O, Coe, Bradley P, Henson, Jessica M, Daza, Riza M, Eichler, Evan E, Shendure, Jay, Gammill, Hilary S

    Published in The New England journal of medicine (23-04-2015)
    “…False positive results for trisomy 18 from DNA-based noninvasive prenatal screening were caused, in two of the four patients who were evaluated, by maternal…”
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