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Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL Yazar: Klintman, J, Barmpouti, K, Knight, S, Robbe, P, Dreau, H, Clifford, R, Ridout, K, Burns, A, Timbs, A, Bruce, D, Antoniou, P, Sosinsky, A, Becq, J, Bentley, D, Hillmen, P, Taylor, J, Caulfield, M, Schuh, A
Baskı/Yayın Bilgisi 2018Conference item -
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Genomic landscape of adult testicular germ cell tumours in the 100,000 Genomes Project Yazar: Ní Leathlobhair, M, Frangou, A, Kinnersley, B, Cornish, AJ, Chubb, D, Lakatos, E, Arumugam, P, Gruber, AJ, Law, P, Tapinos, A, Jakobsdottir, GM, Peneva, I, Sahli, A, Smyth, EM, Ball, RY, Sylva, R, Benes, K, Stark, D, Young, RJ, Lee, ATJ, Wolverson, V, Houlston, RS, Sosinsky, A, Protheroe, A, Wedge, DC, Verrill, C
Baskı/Yayın Bilgisi 2024Journal article