학술논문

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases
Document Type
Article
Author
Kobren, Shilpa NadimpalliBaldridge, DustinVelinder, MattKrier, Joel B.LeBlanc, KimberlyEsteves, CeciliaPusey, Barbara N.Züchner, StephanBlue, ElizabethLee, HaneHuang, AldenBastarache, LisaBican, AnnaCogan, JoyMarwaha, ShrutiAlkelai, AnnaMurdock, David R.Liu, PengfeiWegner, Daniel J.Paul, Alexander J.Acosta, Maria T.Adam, MargaretAdams, David R.Agrawal, Pankaj B.Alejandro, Mercedes E.Alvey, JustinAmendola, LauraAndrews, AshleyAshley, Euan A.Azamian, Mahshid S.Bacino, Carlos A.Bademci, GuneyBaker, EvaBalasubramanyam, AshokBaldridge, DustinBale, JimBamshad, MichaelBarbouth, DeborahBayrak-Toydemir, PinarBeck, AnitaBeggs, Alan H.Behrens, EdwardBejerano, GillBennett, JimmyBerg-Rood, BeverlyBernstein, Jonathan A.Berry, Gerard T.Bican, AnnaBivona, StephanieBlue, ElizabethBohnsack, JohnBonnenmann, CarstenBonner, DevonBotto, LorenzoBoyd, BrennaBriere, Lauren C.Brokamp, EllyBrown, GabrielleBurke, Elizabeth A.Burrage, Lindsay C.Butte, Manish J.Byers, PeterByrd, William E.Carey, JohnCarrasquillo, OlveenChang, Ta Chen PeterChanprasert, SirisakChao, Hsiao-TuanClark, Gary D.Coakley, Terra R.Cobban, Laurel A.Cogan, Joy D.Coggins, MatthewCole, F. SessionsColley, Heather A.Cooper, Cynthia M.Cope, HeidiCraigen, William J.Crouse, Andrew B.Cunningham, MichaelD’Souza, PrecillaDai, HongzhengDasari, SurendraDavis, JoieDaya, Jyoti G.Deardorff, MatthewDell’Angelica, Esteban C.Dhar, Shweta U.Dipple, KatrinaDoherty, DanielDorrani, NaghmehDoss, Argenia L.Douine, Emilie D.Draper, David D.Duncan, LauraEarl, DawnEckstein, David J.Emrick, Lisa T.Eng, Christine M.Esteves, CeciliaFalk, MarniFernandez, LilianaFerreira, CarlosFieg, Elizabeth L.Findley, Laurie C.Fisher, Paul G.Fogel, Brent L.Forghani, IrmanFresard, LaureGahl, William A.Glass, IanGochuico, BernadetteGodfrey, Rena A.Golden-Grant, KatieGoldman, Alica M.Goldrich, Madison P.Goldstein, David B.Grajewski, AlanaGroden, Catherine A.Gutierrez, IrmaHahn, SihounHamid, RizwanHanchard, Neil A.Hassey, KellyHayes, NicholeHigh, FrancesHing, AnneHisama, Fuki M.Holm, Ingrid A.Hom, JasonHorike-Pyne, MarthaHuang, AldenHuang, YongHuryn, LaryssaIsasi, RosarioJamal, FarihaJarvik, Gail P.Jarvik, JeffreyJayadev, SumanKaraviti, LefkotheaKennedy, JenniferKiley, DanaKohane, Isaac S.Kohler, Jennefer N.Korrick, SusanKozuira, MaryKrakow, DeborahKrasnewich, Donna M.Kravets, ElijahKrier, Joel B.LaMoure, Grace L.Lalani, Seema R.Lam, ByronLam, ChristinaLanpher, Brendan C.Lanza, Ian R.Latham, LeaLeBlanc, KimberlyLee, Brendan H.Lee, HaneLevitt, RoyLewis, Richard A.Lincoln, Sharyn A.Liu, PengfeiLiu, Xue ZhongLongo, NicolaLoo, Sandra K.Loscalzo, JosephMaas, Richard L.MacDowall, JohnMacRae, Calum A.Macnamara, Ellen F.Maduro, Valerie V.Majcherska, Marta M.Mak, Bryan C.Malicdan, May Christine V.Mamounas, Laura A.Manolio, Teri A.Mao, RongMaravilla, KennethMarkello, Thomas C.Marom, RonitMarth, GaborMartin, Beth A.Martin, Martin G.Martinez-Agosto, Julian A.Marwaha, ShrutiMcCauley, JacobMcConkie-Rosell, AllynMcCormack, Colleen E.McCray, Alexa T.McGee, ElisabethMefford, HeatherMerritt, J. LawrenceMight, MatthewMirzaa, GhaydaMorava, EvaMoretti, Paolo M.Moretti, PaoloMosbrook-Davis, DeborahMulvihill, John J.Murdock, David R.Nagy, AnnaNakano-Okuno, MarikoNath, AviNelson, Stanley F.Newman, John H.Nicholas, Sarah K.Nickerson, DeborahNieves-Rodriguez, ShirleyNovacic, DonnaOglesbee, DevinOrengo, James P.Pace, LauraPak, StephenPallais, J. CarlPalmer, Christina G.S.Papp, Jeanette C.Parker, Neil H.Phillips, John A.Posey, Jennifer E.Potocki, LorrainePower, BradleyPusey, Barbara N.Quinlan, AaronRaja, Archana N.Rao, Deepak A.Raskind, WendyRenteria, GeneceeReuter, Chloe M.Rives, LynetteRobertson, Amy K.Rodan, Lance H.Rosenfeld, Jill A.Rosenwasser, NatalieRossignol, FrancisRuzhnikov, MauraSacco, RalphSampson, Jacinda B.Samson, Susan L.Saporta, MarioSchaechter, JudySchedl, TimothySchoch, KellyScott, C. RonScott, Daryl A.Shashi, VandanaShin, JimannSigner, Rebecca H.Silverman, Edwin K.Sinsheimer, Janet S.Sisco, KathySmith, Edward C.Smith, Kevin S.Solem, EmilySolnica-Krezel, LiliannaSolomon, BenSpillmann, Rebecca C.Stoler, Joan M.Sullivan, Jennifer A.Sullivan, KathleenSun, AngelaSutton, ShirleySweetser, David A.Sybert, VirginiaTabor, Holly K.Tan, Amelia L.M.Tan, Queenie K.-G.Tekin, MustafaTelischi, FredThorson, WillaThurm, AudreyTifft, Cynthia J.Toro, CamiloTran, Alyssa A.Tucker, Brianna M.Urv, Tiina K.Vanderver, AdelineVelinder, MattViskochil, DaveVogel, Tiphanie P.Wahl, Colleen E.Walker, MelissaWallace, StephanieWalley, Nicole M.Walsh, Chris A.Wambach, JenniferWan, JijunWang, Lee-kaiWangler, Michael F.Ward, Patricia A.Wegner, DanielWener, MarkWenger, TaraPerry, Katherine WesselingWesterfield, MonteWheeler, Matthew T.Whitlock, JordanWolfe, Lynne A.Woods, Jeremy D.Yamamoto, ShinyaYang, JohnYousef, MuhammadZastrow, Diane B.Zein, WadihZhao, ChunliZuchner, StephanSunyaev, Shamil R.Kohane, Isaac S.
Source
Genetics in Medicine; June 2021, Vol. 23 Issue: 6 p1075-1085, 11p
Subject
Language
ISSN
10983600; 15300366
Abstract
Genomic sequencing has become an increasingly powerful and relevant tool to be leveraged for the discovery of genetic aberrations underlying rare, Mendelian conditions. Although the computational tools incorporated into diagnostic workflows for this task are continually evolving and improving, we nevertheless sought to investigate commonalities across sequencing processing workflows to reveal consensus and standard practice tools and highlight exploratory analyses where technical and theoretical method improvements would be most impactful.