100: ALMA: Epigenomic diagnosis & prognosis of AML
Base by Base8 Aug 2025

100: ALMA: Epigenomic diagnosis & prognosis of AML

Marchi F et al., Nature Communications - This study builds the Acute Leukemia Methylome Atlas (ALMA) from 3,314 patient methylomes and presents three models—ALMA Subtype, AML Epigenomic Risk, and a 38‑CpG signature—that classify WHO2022 subtypes and predict 5‑year survival. The authors also demonstrate a nanopore-based specimen‑to‑result workflow for combined genome and epigenome profiling. Key terms: acute myeloid leukemia, DNA methylation, epigenomics, nanopore sequencing, machine learning.

Study Highlights:
The authors harmonized DNA methylation from 3,314 leukemia patient samples (331,556 CpGs) to create ALMA and a PaCMAP‑based representation that supports supervised classifiers. ALMA Subtype accurately stratifies 27 WHO2022 diagnostic subtypes and the AML Epigenomic Risk model predicts 5‑year overall survival with validation across independent pediatric and adult cohorts. A 38‑CpG prognostic signature derived by EWAS and penalized Cox modeling predicts 5‑year OS and remains independently prognostic after multivariable adjustment. A rapid long‑read nanopore specimen‑to‑result protocol on 20 specimens showed high concordance between epigenomic signatures and genomic lesions, with limitations for rare subtypes and very low coverage.

Conclusion:
ALMA and its derived models demonstrate that DNA methylation profiling, combined with machine learning and a nanopore specimen‑to‑result workflow, can improve diagnostic subtyping and 5‑year prognostication in AML, though broader training data and prospective validation are needed for rare subtypes.

Music:
Enjoy the music based on this article at the end of the episode.

Article title:
Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia

First author:
Marchi F

Journal:
Nature Communications

DOI:
10.1038/s41467-025-62005-4

Reference:
Marchi F. et al., Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia. Nature Communications (2025). doi:10.1038/s41467-025-62005-4

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

On PaperCast Base by Base you'll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

Episode link: https://basebybase.com/episodes/alma-epigenomic-aml-episode-100

QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2025-08-08.

QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited the transcript's presentation of ALMA atlas construction, subtype and risk modeling, 38-CpG signature, nanopore specimen-to-result workflow, and discussed limitations. Compared these to the canonical article text.
- transcript topics: ALMA atlas construction and data scale; PaCMAP dimensionality reduction; ALMA Subtype classification across WHO2022; AML Epigenomic Risk prognostic modeling; 38-CpG AML Signature prognostic capability; Nanopore specimen-to-result protocol and clinical validation

QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 7
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0

Metadata Audited:
- article_doi
- article_title
- article_journal
- license

Factual Items Audited:
- ALMA built from 3314 patient samples across 11 harmonized cohorts (331556 CpGs).
- ALMA Subtype classifies 27 WHO2022 subtypes plus otherwise-normal control with robust cross-cohort per...

Denne episoden er hentet fra en åpen RSS-feed og er ikke publisert av Podme. Den kan derfor inneholde annonser.

Episoder(444)

441: Evolutionary mapping of Cav1.3 functional sites

441: Evolutionary mapping of Cav1.3 functional sites

Tang X et al., PNAS - The authors apply an evolutionary sequence-covariation model to the Cav1.3 (CACNA1D) α1-subunit, map predicted pathogenicity onto structural models, and validate five predicted s...

14 Aug 24min

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

Lamkina EN et al., PNAS - This episode reviews a PNAS brief report showing that DENV-4 infection induces marked DNA damage in infected cells while broadly suppressing transcription of DNA repair pathw...

12 Aug 23min

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

Lamkina EN et al., PNAS - This episode reviews a PNAS brief report showing that DENV-4 infection induces marked DNA damage in infected cells while broadly suppressing transcription of DNA repair pathw...

12 Aug 23min

439: Coembedding Sequence and Structure: CLSS Maps the Protein Universe

439: Coembedding Sequence and Structure: CLSS Maps the Protein Universe

Longo LM et al., PNAS - This episode summarizes a PNAS study introducing CLSS, a contrastive two-tower protein language model that coembeds domain sequences, structures, and subsequences into a shared...

11 Aug 23min

438: Mapping AIRE: a proactive atlas of 9,790 missense variants

438: Mapping AIRE: a proactive atlas of 9,790 missense variants

Axakova A et al., The American Journal of Human Genetics - Axakova et al. generated a variant effect map for AIRE using an insulin‑promoter GFP reporter in HEK293 cells to measure the functional impac...

10 Aug 24min

437: Cell villages and Dirichlet modeling map human cell fitness genetics

437: Cell villages and Dirichlet modeling map human cell fitness genetics

Hanson C et al., The American Journal of Human Genetics - Hanson et al. combine pooled multi-donor human neural progenitor cell "villages" with Townlet, a hierarchical Dirichlet regression model, to e...

9 Aug 28min

436: KIAP4 and the ARND family: building the Leishmania adhesion plaque

436: KIAP4 and the ARND family: building the Leishmania adhesion plaque

Owino BO et al., PNAS - Using TurboID proximity proteomics and microscopy, researchers identify KIAP4 as the canonical member of a conserved Adhesion Related NTPase-like Domain (ARND) family that loca...

8 Aug 24min

435: E. coli TGT binds two tRNAs — cryo-EM reveals dual engagement

435: E. coli TGT binds two tRNAs — cryo-EM reveals dual engagement

Ember M et al., PNAS - This episode examines a cryo-EM study of Escherichia coli tRNA-guanine transglycosylase (TGT) that solves the enzyme structure and its covalent intermediate with tRNATyr. Unexpe...

7 Aug 19min

Populært innen Vitenskap

fastlegen
tingenes-tilstand
romkapsel
jss
liberal-halvtime
rekommandert
villmarksliv
abels-tarn
dekodet-2
vett-og-vitenskap-med-gaute-einevoll
sinnsyn
fjellsportpodden
rss-overskuddsliv
rss-rekommandert
tomprat-med-gunnar-tjomlid
rss-inn-til-kjernen-med-sunniva-rose
hva-er-greia-med
rss-nysgjerrige-norge
diagnose
kvinnehelsepodden