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February 12, 2024Open Access

Table S6 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy

Ignacio Campillo‐Marcos Marta Casado-Peláez Verónica Dávalos Gerardo Ferrer Caterina Mata Elisabetta Mereu Gaël Roué David Valcárcel Antonieta Molero Lurdes Zamora Blanca Xicoy Laura Palomo Pamela Acha Ana Manzanares Magnus Tobiasson Eva Hellström‐Lindberg Françesc Solé Manel Esteller

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Abstract

Karyotype and mutations (bulk NGS and single-cell DNAseq) at diagnosis for the studied MDS cases

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Campillo‐Marcos et al. (2024) studied this question.

synapsesocial.com/papers/68e79856b6db643587709015 https://doi.org/10.1158/2767-9764.25206410

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Table S6 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
2Table S1 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
3Table S1 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
4TABLE 1 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
5TABLE 1 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024

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Figure S4 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
FIGURE 2 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024
Table S5 from Single-cell Multiomics Analysis of Myelodysplastic Syndromes and Clinical Response to Hypomethylating Therapy2024