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Minimum sample size for external validation of a clinical prediction model with a binary outcome

Autor: Riley, RD, Debray, TPA, Collins, GS, Archer, L, Ensor, J, van Smeden, M, Snell, KIE

Publikováno v: Statistics in Medicine. 40:4230-4251

In prediction model research, external validation is needed to examine an existing model's performance using data independent to that for model development. Current external validation studies often suffer from small sample sizes and consequently imp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4806814f1f15c7510709d6e406bafed
https://doi.org/10.1002/sim.9025

ETS transcription factor ELF3 (ESE-1) is a cell cycle regulator in benign and malignant prostate

Autor: Archer, L K, Frame, F M, Walker, H F, Droop, A P, McDonald, G L K, Kucko, S, Berney, D M, Mann, V M, Simms, M S, Maitland, N J

This study aimed to elucidate the role of ELF3, an ETS family member in normal prostate growth and prostate cancer. Silencing ELF3 in both benign prostate (BPH-1) and prostate cancer (PC3) cell lines resulted in decreased colony forming ability, inhi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::f5bcc11a2756600a637d3781c2a5faec
https://eprints.whiterose.ac.uk/190322/1/FEBS_Open_Bio_2022_Archer_ETS_transcription_factor_ELF3_ESE_1_is_a_cell_cycle_regulator_in_benign_and_malignant.pdf

Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

Autor: Wai, Htoo A, Lord, Jenny, Lyon, Matthew, Gunning, Adam, Kelly, Hugh, Cibin, Penelope, Seaby, Eleanor G, Spiers-Fitzgerald, Kerry, Lye, Jed, Ellard, Sian, Thomas, N Simon, Bunyan, David J, Douglas, Andrew G L, Baralle, Diana, Naik, Swati, Ragge, Nicola, Cox, Helen, Morton, Jenny E., O'Driscoll, Mary, Lim, Derek, Osio, Deborah, Elmslie, Frances, Huber, Camilla, Hewitt, Julie, Brandon, Heidy, McEntagart, Meriel, Mansour, Sahar, Lahiri, Nayana, Dempsey, Esther, Manalo, Merrie, Homfray, Tessa, Saggar, Anand, Li, Jin, Barwell, Julian, Chandler, Kate E., Briggs, Tracy, Douzgou, Sofia, Adlard, Julian, Kraus, Alison, Mehta, Sarju, Watford, Amy, Donaldson, Alan, Low, Karen, Jones, Gabriela, Dixit, Abhijit, King, Elizabeth, Shannon, Nora, Kaliakatsos, Marios, Joss, Shelagh, Balasubramanian, Meena, Johnson, Diana, Everest, Sarah, Salter, Claire, Harrison, Victoria, Wise, Gillian, Torokwa, Audrey, Sands, Victoria, Pyle, Esther, Thomas, Tessy, Lachlan, Katherine, Foulds, Nicola, Lotery, Andrew, Hammans, Simon R., Pond, Emily, Horton, Rachel, Kharbanda, Mira, Hunt, David, Thomas, Charlene, Side, Lucy, Willis, Catherine, Greville-Heygate, Stephanie, Mawby, Rebecca, Mercer, Catherine, Temple, Karen, Kinning, Esther, Bojovic, Ognjen, Archer, L.

Publikováno v: Genetics in Medicine
Wai, H A, Lord, J, Lyon, M, Gunning, A, Kelly, H, Cibin, P, Seaby, E G, Spiers-Fitzgerald, K, Lye, J, Ellard, S, Thomas, N S, Bunyan, D J, Douglas, A G L, Baralle, D, Splicing and disease working group, Naik, S, Ragge, N, Cox, H, Morton, J E, O'Driscoll, M, Lim, D, Osio, D, Elmslie, F, Huber, C, Hewitt, J, Brandon, H, McEntagart, M, Mansour, S, Lahiri, N, Dempsey, E, Manalo, M, Homfray, T, Saggar, A, Li, J, Barwell, J, Chandler, K E, Briggs, T, Douzgou, S, Adlard, J, Kraus, A, Mehta, S, Watford, A, Donaldson, A, Low, K, Jones, G, Dixit, A, King, E, Shannon, N, Kaliakatsos, M, Manalo, M, Joss, S, Balasubramanian, M, Johnson, D, Everest, S, Salter, C, Harrison, V, Wise, G, Torokwa, A, Sands, V, Pyle, E, Thomas, T, Lachlan, K, Foulds, N, Lotery, A, Douglas, A G L, Hammans, S R, Pond, E, Horton, R, Kharbanda, M, Hunt, D, Thomas, C, Side, L, Willis, C, Greville-Heygate, S, Mawby, R, Mercer, C, Temple, K, Kinning, E, Bojovic, O & Archer, L 2020, ' Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 6, pp. 1005-1014 . https://doi.org/10.1038/s41436-020-0766-9

Diagnosis of genetic disorders is hampered by large numbers of variants of uncertain significance (VUSs) identified through next-generation sequencing. Many such variants may disrupt normal RNA splicing. We examined effects on splicing of a large coh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396f4f2237f59188dc55ecb2a7ba5f4d
https://doi.org/10.1038/s41436-020-0766-9