학술논문

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants
Document Type
Article
Author
Bournazos, Adam M.Riley, Lisa G.Bommireddipalli, ShobhanaAdes, LesleyAkesson, Lauren S.Al-Shinnag, MohammadAlexander, Stephen I.Archibald, Alison D.Balasubramaniam, ShantiBerman, YemimaBeshay, VictoriaBoggs, KirstenBojadzieva, JasminaBrown, Natasha J.Bryen, Samantha J.Buckley, Michael F.Chong, BelindaDavis, Mark R.Dawes, RuebenaDelatycki, MartinDonaldson, LizDownie, LilianEdwards, CaitlinEdwards, MatthewEngel, AmandaEwans, Lisa J.Faiz, FathimathFennell, AndrewField, MichaelFreckmann, Mary-LouiseGallacher, LyndonGear, RussellGoel, HimanshuGoh, ShuxiangGoodwin, LindaHanna, BernadetteHarraway, JamesHiggins, MeganHo, GladysHopper, Bruce K.Horton, Ari E.Hunter, Matthew F.Huq, Aamira J.Josephi-Taylor, SarahJoshi, HimanshuKirk, EdwinKrzesinski, EmmaKumar, Kishore R.Lemckert, FrancesLeventer, Richard J.Lindsey-Temple, Suzanna E.Lunke, SebastianMa, AlanMacaskill, StevenMallawaarachchi, AmaliMarty, MelanieMarum, Justine E.McCarthy, Hugh J.Menezes, Manoj P.McLean, AlisonMilnes, DiMohammad, ShekeebMowat, DavidNiaz, AramPalmer, Elizabeth E.Patel, ChiragPatel, Shilpan G.Phelan, DeanPinner, Jason R.Rajagopalan, SulekhaRegan, MatthewRodgers, JonathanRodrigues, MiriamRoxburgh, Richard H.Sachdev, RaniRoscioli, TonySamarasekera, RuvishaniSandaradura, Sarah A.Savva, ElenaSchindler, TimShah, MargitSinnerbrink, Ingrid B.Smith, Janine M.Smith, Richard J.Springer, AmandaStark, ZornitzaStrom, Samuel P.Sue, Carolyn M.Tan, KennethTan, Tiong Y.Tantsis, EstherTchan, Michel C.Thompson, Bryony A.Trainer, Alison H.van Spaendonck-Zwarts, KarinWalsh, RebeccaWarwick, LindaWhite, StephanieWhite, Susan M.Williams, Mark G.Wilson, Meredith J.Wong, Wui KwanWright, Dale C.Yap, PatrickYeung, AlisonYoung, HelenJones, Kristi J.Bennetts, BruceCooper, Sandra T.Abdulrasool, GhusoonAkesson, Lauren S.Al Eryani, GhamdanAl-Shinnag, MohammadArts, PeerBagnall, RichardBaker, Naomi L.Barnett, ChristopherBeecroft, SarahBennetts, BruceBerbic, MarinaBeshay, VictoriaBlack, MichaelBlackburn, JimBlombery, PiersBoggs, KirstenBournazos, Adam M.Branford, SusanBreen, JimmyBrown, Natasha J.Bryen, Samantha J.Burnett, LeslieCanson, DaffodilCheong, PakChew, EdwardChong, BelindaChristodoulou, JohnChung, Seo-KyungClark, MikeCliffe, CorrinaCole, MelissaCollins, FelicityCompton, AlisonCooper, AntonyCooper, Sandra T.Corbett, MarkCowley, MarkDavis, Mark R.Delatycki, MartinDudding, TracyEdwards, MatthewEggers, StefanieEwans, Lisa J.Eyras, EduardoFaiz, FathimathFernandez, Miriam FanjulFellowes, AndrewFennell, AndrewField, MichaelFleischer, RonFolland, ChiaraFox, LucyFreckmann, Mary-LouiseGaff, ClaraGalea, MelanieGhaoui, RoulaGoel, HimanshuGornanitis, IliasHa, ThuongHanna, BernadetteHarraway, JamesHayashi, RippeiHayes, IanHenderson, AlexHesson, LukeHeyer, ErinHildebrand, MichaelHipwell, MichaelHo, GladysHorton, Ari E.Hoskins, CassHunter, Matthew F.Jackson, MatildaJames, PaulJones, Kristi J.Wong, Justin Jong-LeongJosephi-Taylor, SarahJoshi, HimanshuKassahn, KarinKaub, PeterKevin, LucyKirk, EdwinKrzesinski, EmmaKumble, SmithaKummerfeld, SarahLaing, NigelLau, ChiyanLee, EricLeighton, SarahLundie, BenLunke, SebastianMallawaarachchi, AmaliMayoh, ChelseaMcGaughran, JulieMcLean, AlisonMcPhillips, MaryMeldrum, CliffMiddleton, EdwinaMilnes, DiMina, KymMowat, DavidNisselle, AmyOates, EmilyOshlack, AliciaPalmer, Elizabeth E.Parasivam, GayathriParsons, MichaelPatel, ChiragPinner, Jason R.Quinn, MichaelRasko, JohnRavenscroft, GinaRavine, AnjaRecsei, KristaRegan, MatthewRehn, JacquelineRiley, Lisa G.Robertson, StephenRonan, AnneRoscioli, TonyRyland, GeorginaSadedin, SimonSandaradura, Sarah A.Schreiber, AndreasScott, HamishScott, RodneySemsarian, ChristopherSimons, CasSinger, EmmaSmith, Janine M.Smyth, ReneeSpurdle, AmandaStark, ZornitzaSullivan, PatriciaSundercombe, SamanthaTan, Tiong Y.Tchan, Michel C.Thompson, Bryony A.Thorburn, DavidToubia, JohnTrent, RonaldTudini, EmmaVoneague, IrinaWaddell, LeighWalker, LoganWallis, MathewWarnock, NickWeatheritt, RobertWhite, DeborahWhite, Susan M.Williams, Mark G.Wilson, Meredith J.Winship, IngridWorgan, LisaWright, Dale C.Wu, KathyYeung, AlisonZiolowski, Andrew
Source
Genetics in Medicine; January 2022, Vol. 24 Issue: 1 p130-145, 16p
Subject
Language
ISSN
10983600; 15300366
Abstract
Genetic variants causing aberrant premessenger RNA splicing are increasingly being recognized as causal variants in genetic disorders. In this study, we devise standardized practices for polymerase chain reaction (PCR)-based RNA diagnostics using clinically accessible specimens (blood, fibroblasts, urothelia, biopsy).