Works matching IS 17558794 AND DT 2016 AND VI 9


Results: 67
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    Pitfalls of improperly procured adjacent non-neoplastic tissue for somatic mutation analysis using next-generation sequencing.

    Published in:
    BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0226-1
    By:
    • Lei Wei;
    • Papanicolau-Sengos, Antonios;
    • Song Liu;
    • Jianmin Wang;
    • Conroy, Jeffrey M.;
    • Glenn, Sean T.;
    • Brese, Elizabeth;
    • Qiang Hu;
    • Miles, Kiersten Marie;
    • Burgher, Blake;
    • Qin, Maochun;
    • Head, Karen;
    • Omilian, Angela R.;
    • Bshara, Wiam;
    • Krolewski, John;
    • Trump, Donald L.;
    • Johnson, Candace S.;
    • Morrison, Carl D.
    Publication type:
    Article
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    Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.

    Published in:
    BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0220-7
    By:
    • Morin, Andréanne;
    • Kwan, Tony;
    • Bing Ge;
    • Letourneau, Louis;
    • Ban, Maria;
    • Tandre, Karolina;
    • Caron, Maxime;
    • Sandling, Johanna K.;
    • Carlsson, Jonas;
    • Bourque, Guillaume;
    • Laprise, Catherine;
    • Montpetit, Alexandre;
    • Syvanen, Ann-Christine;
    • Ronnblom, Lars;
    • Sawcer, Stephen J.;
    • Lathrop, Mark G.;
    • Pastinen, Tomi
    Publication type:
    Article
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    Explorations to improve the completeness of exome sequencing.

    Published in:
    BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0216-3
    By:
    • Chen Du;
    • Pusey, Barbara N.;
    • Adams, Christopher J.;
    • Lau, C. Christopher;
    • Bone, William P.;
    • Gahl, William A.;
    • Markello, Thomas C.;
    • Adams, David R.
    Publication type:
    Article
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    eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.

    Published in:
    BMC Medical Genomics, 2016, v. 9, p. 19, doi. 10.1186/s12920-016-0191-8
    By:
    • Verma, Anurag;
    • Verma, Shefali S.;
    • Pendergrass, Sarah A.;
    • Crawford, Dana C.;
    • Crosslin, David R.;
    • Kuivaniemi, Helena;
    • Bush, William S.;
    • Bradford, Yuki;
    • Kullo, Iftikhar;
    • Bielinski, Suzette J.;
    • Rongling Li;
    • Denny, Joshua C.;
    • Peissig, Peggy;
    • Hebbring, Scott;
    • De Andrade, Mariza;
    • Ritchie, Marylyn D.;
    • Tromp, Gerard
    Publication type:
    Article
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    Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate.

    Published in:
    BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0208-3
    By:
    • Wu-Lin Charng;
    • Karaca, Ender;
    • Coban Akdemir, Zeynep;
    • Gambin, Tomasz;
    • Atik, Mehmed M.;
    • Shen Gu;
    • Posey, Jennifer E.;
    • Jhangiani, Shalini N.;
    • Muzny, Donna M.;
    • Doddapaneni, Harsha;
    • Jianhong Hu;
    • Boerwinkle, Eric;
    • Gibbs, Richard A.;
    • Rosenfeld, Jill A.;
    • Hong Cui;
    • Fan Xia;
    • Manickam, Kandamurugu;
    • Yaping Yang;
    • Faqeih, Eissa A.;
    • Al Asmari, Ali
    Publication type:
    Article
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