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. 2023 Mar 3;212(3):262–275. doi: 10.1093/cei/uxad034

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© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Immunology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — MALAT1 anti-correlates to genes that are related to cell cycle progression in T cells. (A) Network representation of STRING interactions plotted for top 100 MALAT1 anti-correlated genes and those that are common in CD4+ and CD8+ T cells with lines indicating interconnectedness in terms of co-expression or interaction. (B) Barplots showing negative log FDR values for HALLMARK GSEA enrichment for genes that anti-correlate with MALAT1 and those that are uniquely so in CD4+ and CD8+ T cells. The ‘x’ axis contains HALLMARK gene set names that were found to enriched. (C) Same as A but for top 20 unique genes for CD4+ T cells. (D) Network representation of STRING interactions for top 20 unique CD8+ T cells.