Preprint > Page 14
  • bioRxiv  ·  May 14, 2024  ·  Preprint

    Low copy CRISPR-Cas13d mitigates collateral RNA cleavage.

    Sydney K. Hart, Hans-Hermann Wessels, Alejandro Méndez-Mancilla, Simon Müller, Gediminas Drabavicius, Olivia Choi, Neville E. Sanjana

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  • arXiv  ·  April 29, 2024  ·  Preprint

    A Universal Metric of Dataset Similarity for Cross-silo Federated Learning.

    Ahmed Elhussein and Gamze Gürsoy

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  • bioRxiv  ·  April 26, 2024  ·  Preprint

    Tissue and cellular spatiotemporal dynamics in colon aging.

    Aidan C. Daly, Francesco Cambuli, Tarmo Äijö, Britta Lötstedt, Nemanja Marjanovic, Olena Kuksenko, Matthew Smith-Erb, Sara Fernandez, Daniel Domovic, Nicholas Van Wittenberghe, Eugene Drokhlyansky, Gabriel K Griffin, Hemali Phatnani, Richard Bonneau, Aviv Regev, Sanja Vicković

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  • bioRxiv  ·  April 20, 2024  ·  Preprint

    Ultra-secure storage and analysis of genetic data for the advancement of precision medicine.

    Jacob Blindenbach, Jiayi Kang, Seungwan Hong, Caline Karam, Thomas Lehner, Gamze Gürsoy

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  • bioRxiv  ·  March 14, 2024  ·  Preprint

    Enhancer-targeted CRISPR-Activation Rescues Haploinsufficient Autism Susceptibility Genes.

    eGeorge T Chen, Gayatri Nair, Aubrey J Osorio, Sandra M Holley, Kimiya Ghassemzadeh, Jose G Gonzalez, Congyi Lu, Neville E Sanjana, Carlos Cepeda, Daniel Geschwind

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  • bioRxiv  ·  March 7, 2024  ·  Preprint

    Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.

    Jonas A. Gustafson, Sophia B. Gibson, Nikhita Damaraju, Miranda PG Zalusky, Kendra Hoekzema, David Twesigomwe, Lei Yang, Anthony A. Snead, Phillip A. Richmond, Wouter De Coster, Nathan D. Olson, Andrea Guarracino, Qiuhui Li, Angela L. Miller, Joy Goffena, Zachery Anderson, Sophie HR Storz, Sydney A. Ward, Maisha Sinha, Claudia Gonzaga-Jauregui, Wayne E. Clarke, Anna O. Basile, André Corvelo, Catherine Reeves, Adrienne Helland, Rajeeva Lochan Musunuri, Mahler Revsine, Karynne E. Patterson, Cate R. Paschal, Christina Zakarian, Sara Goodwin, Tanner D. Jensen, Esther Robb, The 1000 Genomes ONT Sequencing Consortium, University of Washington Center for Rare Disease Research (UW-CRDR), Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium, W. Richard McCombie, Fritz J. Sedlazeck, Justin M. Zook, Stephen B. Montgomery, Erik Garrison, Mikhail Kolmogorov, Michael C. Schatz, Richard N. McLaughlin Jr., Harriet Dashnow, Michael C. Zody, Matt Loose, Miten Jain, Evan E. Eichler, Danny E. Miller

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  • bioRxiv.  ·  February 11, 2024  ·  Preprint

    The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARI.

    Liubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, Kevin Shi, Chris Fleisch, Nikolay Dimitrov, Svetlin Mladenov, Simon Xu, Jake Hall, Steven Ford, Yoon-ha Lee, Boris Yamrom, Steven Marks, Adriana Munoz, Alex Lash, Natalia Volfovsky, Ivan Iossifov.

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  • bioRxiv  ·  December 31, 2023  ·  Preprint

    Specifying cellular context of transcription factor regulons for exploring context-specific gene regulation programs.

    Mariia Minaeva, Julia Domingo, Philipp Rentzsch, Tuuli Lappalainen

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  • bioRxiv  ·  December 26, 2023  ·  Preprint

    CRISPRmap: Sequencing-free optical pooled screens mapping multi-omic phenotypes in cells and tissue.

    Jiacheng Gu, Abhishek Iyer, Ben Wesley, Angelo Taglialatela, Giuseppe Leuzzi, Sho Hangai, Aubrianna Decker, Ruoyu Gu, Naomi Klickstein, Yuanlong Shuai, Kristina Jankovic, Lucy Parker-Burns, Yinuo Jin, Jia Yi Zhang, Justin Hong, Steve Niu, Jacqueline Chou, Dan A. Landau, Elham Azizi, Edmond M. Chan, Alberto Ciccia, Jellert T. Gaublomme

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