Tumor evolution modeling in transformed and progressed follicular lymphoma patients.
- Robert Kridel (3396272)
- Fong Chun Chan (3396242)
- Anja Mottok (107742)
- Merrill Boyle (3396254)
- Pedro Farinha (3396269)
- King Tan (3396263)
- Barbara Meissner (220869)
- Ali Bashashati (757758)
- Andrew McPherson (220794)
- Andrew Roth (734870)
- Karey Shumansky (453617)
- Damian Yap (468619)
- Susana Ben-Neriah (3396260)
- Jamie Rosner (3396266)
- Maia A. Smith (841132)
- Cydney Nielsen (3396245)
- Eva Giné (3396251)
- Adele Telenius (3396239)
- Daisuke Ennishi (3396248)
- Andrew Mungall (3396257)
- Richard Moore (2297)
- Ryan D. Morin (726476)
- Nathalie A. Johnson (3396275)
- Laurie H. Sehn (3396236)
- Thomas Tousseyn (482297)
- Ahmet Dogan (135774)
- Joseph M. Connors (184867)
- David W. Scott (344608)
- Christian Steidl (482300)
- Marco A. Marra (53809)
- Randy D. Gascoyne (103838)
- Sohrab P. Shah (220828)
Publication date
December 2016
DOIAbstract
<p>Genetic drift modeling in TFL (A) and PFL (B) patients with an initial variant allele frequency of 1% and 50%, respectively. The far left bar plot indicates the number of simulations that follow a specific genetic drift trajectory (shown on the right). PFL, progressed follicular lymphoma; TFL, transformed follicular lymphoma; VAF, variant allele frequency.</p
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