Copy number signatures predict chromothripsis and clinical outcomes in newly diagnosed multiple myeloma
Chromothripsis is associated with unfavourable outcomes in multiple myeloma (MM), but its detection usually requires whole genome sequencing. Here the authors develop an approach to detect chromothripsis in MM based on copy-number signatures that also works with whole exome sequencing data.
Saved in:
Main Authors: | Kylee H. Maclachlan, Even H. Rustad, Andriy Derkach, Binbin Zheng-Lin, Venkata Yellapantula, Benjamin Diamond, Malin Hultcrantz, Bachisio Ziccheddu, Eileen M. Boyle, Patrick Blaney, Niccolò Bolli, Yanming Zhang, Ahmet Dogan, Alexander M. Lesokhin, Gareth J. Morgan, Ola Landgren, Francesco Maura |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/b5e6a8716f6d4f72afb2988be3482362 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
mmsig: a fitting approach to accurately identify somatic mutational signatures in hematological malignancies
by: Even H. Rustad, et al.
Published: (2021) -
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities
by: Bénedith Oben, et al.
Published: (2021) -
The landscape of chromothripsis across adult cancer types
by: Natalia Voronina, et al.
Published: (2020) -
Accelerated single cell seeding in relapsed multiple myeloma
by: Heather J. Landau, et al.
Published: (2020) -
Author Correction: Accelerated single cell seeding in relapsed multiple myeloma
by: Heather J. Landau, et al.
Published: (2021)