<?xml version="1.0" encoding="UTF-8"?> <rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"> <channel> <title>CHEN, Yiru - Research Radar</title> <link>https://CHENyiru3.github.io/research-radar/</link> <atom:link href="https://CHENyiru3.github.io/research-radar/feed.xml" rel="self" type="application/rss+xml"/> <description>Daily ranked academic article recommendations from Research Radar.</description> <language>en</language> <lastBuildDate>Tue, 28 Apr 2026 14:03:48 +0000</lastBuildDate> <item> <title>[Computational #1] Interpretable, flexible and spatially aware integration of multiple spatial transcriptomics datasets from diverse sources</title> <link>https://www.nature.com/articles/s41588-026-02579-x</link> <guid isPermaLink="false">2026-04-28-comp-1-10.1038/s41588-026-02579-x</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Computational | Source: Nature Genetics | Published: 2026-04-27 | DOI: 10.1038/s41588-026-02579-x | Recommendation: READ FULL | Summary: INSPIRE combines deep learning with non-negative matrix factorization to integrate diverse spatial transcriptomics datasets, recovering shared and context-specific spatial gene programs and tissue organization across scales. | Why it matters: Cross-platform spatial integration is a central bottleneck. INSPIRE&apos;s interpretable factorization is a strong alternative to black-box embeddings when biological programs must be compared across cohorts.</description> <category>spatial transcriptomics</category> <category>deep learning</category> <category>NMF</category> <category>cross-dataset integration</category> </item> <item> <title>[Computational #2] Dango: Predicting higher-order genetic interactions</title> <link>https://www.cell.com/cell-systems/fulltext/S2405-4712(26)00075-X?rss=yes</link> <guid isPermaLink="false">2026-04-28-comp-2-https://www.cell.com/cell-systems/fulltext/S2405-4712(26)00075-X?rss=yes</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Computational | Source: Cell Systems | Published: 2026-04-24 | DOI: | Recommendation: READ FULL | Summary: DANGO uses a self-attention hypergraph neural network integrating multimodal molecular networks and protein sequence embeddings to predict higher-order genetic interactions, expanding the yeast trigenic interaction landscape to over 400 million interactions. | Why it matters: Higher-order interactions are combinatorially intractable to measure; predictive graph models make perturbation landscapes computationally navigable.</description> <category>genetic interactions</category> <category>hypergraph neural networks</category> <category>self-attention</category> <category>genotype-to-phenotype</category> </item> <item> <title>[Computational #3] Learning multi-cellular representations of single-cell transcriptomics data enables characterization of patient-level disease states</title> <link>https://www.cell.com/cell-systems/fulltext/S2405-4712(26)00052-9?rss=yes</link> <guid isPermaLink="false">2026-04-28-comp-3-https://www.cell.com/cell-systems/fulltext/S2405-4712(26)00052-9?rss=yes</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Computational | Source: Cell Systems | Published: 2026-03-31 | DOI: | Recommendation: READ FULL | Summary: PaSCient learns sample-level representations from single-cell RNA-seq across disease and tissue contexts, highlighting cells and genes that predict patient-level phenotypes such as disease severity and drug response. | Why it matters: Single-cell foundation models operate at cell level, but clinical translation requires patient-level representations. This directly addresses that scale mismatch.</description> <category>single-cell</category> <category>foundation models</category> <category>patient-level phenotypes</category> <category>representation learning</category> </item> <item> <title>[Biomedicine #1] Spatial 5mC-seq profiling of embryos and decidua after implantation in mammals</title> <link>https://www.nature.com/articles/s41592-026-03079-w</link> <guid isPermaLink="false">2026-04-28-biomed-1-10.1038/s41592-026-03079-w</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Biomedicine | Source: Nature Methods | Published: 2026-04-27 | DOI: 10.1038/s41592-026-03079-w | Recommendation: READ FULL | Summary: Spatial 5mC-seq enables unbiased spatiotemporal genome-wide methylome profiling at single-cell resolution in mammalian embryos and decidua. | Why it matters: Expands spatial omics beyond transcript measurements into the methylome, opening a new axis for linking cell state with spatial context.</description> <category>spatial epigenomics</category> <category>DNA methylation</category> <category>single-cell resolution</category> <category>development</category> </item> <item> <title>[Biomedicine #2] Reference-free discovery with barcoded single-cell sequencing</title> <link>https://www.nature.com/articles/s41587-026-03084-6</link> <guid isPermaLink="false">2026-04-28-biomed-2-10.1038/s41587-026-03084-6</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Biomedicine | Source: Nature Biotechnology | Published: 2026-04-22 | DOI: 10.1038/s41587-026-03084-6 | Recommendation: READ FULL | Summary: sc-SPLASH extends reference-free analysis to barcoded single-cell and spatial transcriptomics data, reducing dependence on fixed annotations and prior marker sets. | Why it matters: Reference-free discovery is essential when annotations are incomplete or biased — a recurring limitation in exploratory single-cell and spatial analyses.</description> <category>single-cell</category> <category>spatial transcriptomics</category> <category>reference-free</category> <category>bioinformatics</category> </item> <item> <title>[Biomedicine #3] Sialylated CD43 forms a glyco-immune barrier that restrains antileukemic immunity</title> <link>https://www.science.org/doi/10.1126/science.ady5196</link> <guid isPermaLink="false">2026-04-28-biomed-3-10.1126/science.ady5196</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Biomedicine | Source: Science | Published: 2026-04-09 | DOI: 10.1126/science.ady5196 | Recommendation: READ FULL | Summary: CRISPR knockout screens in human AML cells identify sialylated CD43 as a glyco-immune barrier that restrains macrophage-mediated antileukemic immunity. | Why it matters: Macrophage-directed immunotherapy has struggled clinically; a specific tumor glycosylation barrier provides a concrete mechanism and intervention axis.</description> <category>tumor immunology</category> <category>macrophage phagocytosis</category> <category>CRISPR screen</category> <category>glycosylation</category> </item> <item> <title>[Biomedicine #4] A convergent uPAR-positive tumor ecosystem creates broad vulnerability to CAR T cell therapy</title> <link>https://www.cell.com/cell/fulltext/S0092-8674(26)00269-2?rss=yes</link> <guid isPermaLink="false">2026-04-28-biomed-4-https://www.cell.com/cell/fulltext/S0092-8674(26)00269-2?rss=yes</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Biomedicine | Source: Cell | Published: 2026-03-30 | DOI: | Recommendation: READ FULL | Summary: uPAR CAR T cells synergize with senescence-inducing therapies to eradicate primary and metastatic solid tumors by targeting both tumor cells and supportive stroma, with minimal myelodepletion. | Why it matters: Solid-tumor CAR T needs targets that capture tumor and stromal compartments; a convergent ecosystem vulnerability suggests broader efficacy than tumor-cell-only antigens.</description> <category>CAR T</category> <category>solid tumors</category> <category>tumor ecosystem</category> <category>stroma</category> <category>senescence</category> </item> <item> <title>[Biomedicine #5] Global genetic interaction network of a human cell maps conserved principles and informs functional interpretation of gene co-essentiality profiles</title> <link>https://www.cell.com/cell/fulltext/S0092-8674(26)00345-4?rss=yes</link> <guid isPermaLink="false">2026-04-28-biomed-5-https://www.cell.com/cell/fulltext/S0092-8674(26)00345-4?rss=yes</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Biomedicine | Source: Cell | Published: 2026-04-27 | DOI: | Recommendation: READ FULL | Summary: CRISPR perturbation of ~4 million gene pairs in human HAP1 cells maps ~89,000 genetic interactions, revealing a hierarchical network linking genes to complexes, pathways, and cellular processes while elucidating cancer cell dependencies. | Why it matters: A human-scale genetic interaction map is a foundational resource for interpreting co-essentiality, pathway structure, and synthetic vulnerability.</description> <category>genetic interactions</category> <category>CRISPR screen</category> <category>functional genomics</category> <category>cancer dependencies</category> </item> <item> <title>[Other Fields #1] Today&apos;s robots walk, swim, fly, and manipulate objects on the go — and they&apos;re just getting started</title> <link>https://www.science.org/doi/10.1126/science.aeg9576</link> <guid isPermaLink="false">2026-04-28-field-1-10.1126/science.aeg9576</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Other Fields | Source: Science | Published: 2026-04-16 | DOI: 10.1126/science.aeg9576 | Recommendation: SKIM | Summary: Recent advances in AI-driven control systems have enabled robots to transition between rolling, walking, flying, and swimming — and to use legs as manipulators while moving. This review covers the control challenges overcome to achieve multi-modal locomotion. | Why it matters: Multi-modal robots represent a convergence of AI, control theory, and mechanical engineering — a milestone toward general-purpose embodied intelligence.</description> <category>robotics</category> <category>AI control systems</category> <category>locomotion</category> <category>manipulation</category> </item> <item> <title>[Other Fields #2] AIs can &apos;memorize&apos; data they shouldn&apos;t. Can they be forced to forget?</title> <link>https://www.science.org/content/article/ais-can-memorize-data-they-shouldn-t-can-they-be-forced-forget</link> <guid isPermaLink="false">2026-04-28-field-2-https://www.science.org/content/article/ais-can-memorize-data-they-shouldn-t-can-they-be-forced-forget</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Other Fields | Source: Science | Published: 2026-04-06 | DOI: | Recommendation: SKIM | Summary: A new tool helps researchers probe how large language models &apos;unlearn&apos; sensitive training material, addressing a core tension between model capability and data privacy. | Why it matters: Machine unlearning is becoming a practical requirement as models are trained on increasingly broad data. This work addresses a key AI safety and privacy challenge.</description> <category>machine unlearning</category> <category>AI safety</category> <category>data privacy</category> <category>LLMs</category> </item> <item> <title>[Other Fields #3] Higher education must bridge the AI gap</title> <link>https://www.science.org/doi/10.1126/science.aeh5777</link> <guid isPermaLink="false">2026-04-28-field-3-10.1126/science.aeh5777</guid> <pubDate>Tue, 28 Apr 2026 13:45:00 +0000</pubDate> <description>Section: Other Fields | Source: Science | Published: 2026-04-02 | DOI: 10.1126/science.aeh5777 | Recommendation: SKIM | Summary: As AI advances at a pace that outstrips regulatory and ethical frameworks, this editorial argues that higher education must develop students who can critically engage with AI systems rather than merely use them. | Why it matters: The AI literacy gap in higher education affects how the next generation of scientists and engineers will interact with AI — a structural challenge that shapes all fields.</description> <category>AI in education</category> <category>higher education</category> <category>AI literacy</category> <category>policy</category> </item> </channel> </rss>