Publication > Page 69
  • Nature Methods  ·  August 31, 2017

    GUIDES: sgRNA design for loss-of-function screens.

    Meier, JA, Zhang F, Sanjana, NE.
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  • Neurology Genetics  ·  July 11, 2017

    Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.

    Wrzeszczynski KO, Frank MO, Koyama T, Rhrissorrakrai K, Robine N, Utro F, Emde AK, Chen BJ, Arora K, Shah M, Vacic V, Norel R, Bilal E, Bergmann EA, Moore Vogel JL, Bruce JN, Lassman AB, Canoll P, Grommes C, Harvey S, Parida L, Michelini VV, Zody MC, Jobanputra V, Royyuru AK, Darnell RB.

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  • Genome Research  ·  September 8, 2017

    Detection of long repeat expansions from PCR-free whole-genome sequence data

    Dolzhenko E, van Vugt JJFA, Shaw RJ, Bekritsky MA, van Blitterswijk M, Narzisi G, Ajay SS, Rajan V, Kingsbury Z, Humphray SJ, Schellevis RD, Brands WJ, Baker M, Rademakers R, Kooyman M, Tazelaar GHP, van Es MA, McLaughlin R, Sproviero W, Shatunov A, Jones A, Khleifat AA, Pittman A, Morgan S, Hardiman O, Al-Chalabi A, Shaw C, Smith B, Neo EJ, Morrison K, Shaw PJ, Reeves C, Winterkorn L, Wexler, NS The US-Venezuela Collaborative Research Group, Housman DE, Ng C, Li A, Taft RJ, van den Berg LH, Bentley DR, Veldink JH, Eberle MA

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  • Nature Biotechnology  ·  April 2, 2018

    Integrated analysis of single cell transcriptomic data across conditions, technologies, and species

    Butler A, Hoffman P, Smibert P, Papalexi E, Satija R.

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  • Nature Reviews Genetics  ·  July 3, 2017

    The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain.

    Jiang Y, Loh YE, Rajarajan P, Hirayama T, Liao W, Kassim BS, Javidfar B, Hartley BJ, Kleofas L, Park RB, Labonte B, Ho SM, Chandrasekaran S, Do C, Ramirez BR, Peter CJ, C W JT, Safaie BM, Morishita H, Roussos P, Nestler EJ, Schaefer A, Tycko B, Brennand KJ, Yagi T, Shen L, Akbarian S.

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  • Nature Cell Biology  ·  June 3, 2019

    A single cell transcriptional roadmap for cardiopharyngeal fate diversification

    Wang W, Niu X, Stuart T, Jullian E, Mauck WM, Kelly RG, Satija R, Christiaen L.

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  • Nature Reviews Genetics  ·  May 30, 2017

    Associating cellular epigenetic models with human phenotypes.

    Lappalainen T, Greally JM.

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  • Nature Genetics  ·  May 15, 2017

    PGBD5 promotes site-specific oncogenic mutations in human tumors.

    Henssen AG, Koche R, Zhuang J, Jiang E, Reed C, Eisenberg A, Still E, MacArthur I, Rodríguez-Fos, Gonzalez S, Puiggròs M, Blackford AN, Mason CE, de Stanchina E, Gönen M, Emde A-K, Shah M, Arora K, Reeves C, Socci, ND, Perlman E, Antonescu, CR, Roberts, CWM, Steen H, Mullen E, Jackson SP, Torrent D, Weng Z, Armstrong SA & Kentsis, A.

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  • PLoS Genetics  ·  April 28, 2017

    Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

    Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YM, Auer PL, Laurie CA, Taylor KD, Browning BL, Li Y, Papanicolaou G, Rotter JI, Kurita R, Nakamura Y, Browning SR, Loos RJF, North KE, Laurie CC, Thornton TA, Pankratz N, Bauer DE, Sofer T, Reiner AP.

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  • Bioinformatics  ·  March 11, 2017

    DNA Compass: a secure, client-side site for navigating personal genetic information.

    Curnin C, Gordon A, Erlich Y.

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