光热生物 — 免费癌症多组学在线分析平台 | GRSWSci Cancer Multi-omics Analysis Platform

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    分析摘要

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    分析帮助
    光热生物 使用手册
    TCGA 组学类型说明
    方法全称说明与特点
    转录组数据 (RNA-seq)
    TPMTranscripts Per Million每百万转录本计数。推荐用于样本间比较,已校正基因长度和测序深度,同一样本内所有基因TPM总和为100万
    FPKMFragments Per Kilobase Million每千碱基每百万片段。经典标准化方法,校正基因长度和测序深度,适合单样本内基因表达比较
    FPKM_UQFPKM Upper QuartileFPKM上四分位数标准化。使用75%分位数进行标准化,对极端值更稳健,适合样本间比较
    RSEMRNA-Seq by Expectation-Maximization期望最大化算法估计值。处理多重比对reads,提供更准确的转录本定量,TCGA默认方法
    COUNTS_UNSTRANDEDUnstranded Counts非链特异性原始计数。未标准化的reads计数,适合差异表达分析(如DESeq2)
    COUNTS_STRANDED_FIRSTFirst Strand Counts第一链特异性计数。保留第一链信息的原始计数,用于链特异性文库
    COUNTS_STRANDED_SECONDSecond Strand Counts第二链特异性计数。保留第二链信息的原始计数,用于反向链特异性文库
    TCGA 临床变量说明

    不同肿瘤类型可用的临床变量不同,以下列出本平台已清洗并支持的全部变量及其适用范围。小写肿瘤名为亚型(如 brca_tnbc = 三阴性乳腺癌)。

    病理分级分期

    变量名称中文名肿瘤数适用肿瘤类型
    histological_grade组织学分级28BLCA, CESC, cesc_cscc, CHOL, ESCA, esca_eac, esca_escc, GIC, GLIOMA, HNSC, hnsc_lscc, hnsc_oscc, KIRC, KRCC, LGG, lgg_astrocytoma, lgg_oligoastrocytoma, lgg_oligodendroglioma, LIHC, OV, PAAD, paad_padc, STAD, stad_dga, stad_srcc, UCEC, ucec_eea, ucec_sea
    ajcc_pathologic_stage_clean病理分期42ACC, BLCA, BRCA, brca_idc, brca_ilc, brca_tnbc, CHOL, COAD, coad_lcc, coad_mac, coad_rcc, CRC, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KICH, KIRC, KIRP, KRCC, LIHC, LUAD, LUSC, MESO, NSCLC, PAAD, paad_padc, READ, SKCM, skcm_mcm, skcm_pcm, STAD, stad_dga, stad_srcc, TGCT, tgct_seminoma, THCA, thca_cptc, UVM
    ajcc_pathologic_t_clean原发肿瘤T分期45ACC, BLCA, BRCA, brca_idc, brca_ilc, brca_tnbc, CESC, cesc_cscc, CHOL, COAD, coad_lcc, coad_mac, coad_rcc, CRC, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KICH, KIRC, KIRP, KRCC, LIHC, LUAD, LUSC, MESO, NSCLC, PAAD, paad_padc, PRAD, READ, SKCM, skcm_mcm, skcm_pcm, STAD, stad_dga, stad_srcc, TGCT, tgct_seminoma, THCA, thca_cptc, UVM
    ajcc_pathologic_n_clean淋巴结N分期45ACC, BLCA, BRCA, brca_idc, brca_ilc, brca_tnbc, CESC, cesc_cscc, CHOL, COAD, coad_lcc, coad_mac, coad_rcc, CRC, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KICH, KIRC, KIRP, KRCC, LIHC, LUAD, LUSC, MESO, NSCLC, PAAD, paad_padc, PRAD, READ, SKCM, skcm_mcm, skcm_pcm, STAD, stad_dga, stad_srcc, TGCT, tgct_seminoma, THCA, thca_cptc, UVM
    ajcc_pathologic_m_clean远处转移M分期43BLCA, BRCA, brca_idc, brca_ilc, brca_tnbc, CESC, cesc_cscc, CHOL, COAD, coad_lcc, coad_mac, coad_rcc, CRC, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KICH, KIRC, KIRP, KRCC, LIHC, LUAD, LUSC, MESO, NSCLC, PAAD, paad_padc, READ, SKCM, skcm_mcm, skcm_pcm, STAD, stad_dga, stad_srcc, TGCT, tgct_seminoma, THCA, thca_cptc, UVM
    ajcc_clinical_stage_clean临床分期12ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KIRP, KRCC, TGCT, tgct_seminoma, UVM
    ajcc_clinical_t_clean临床T分期14BLCA, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KIRP, KRCC, PRAD, TGCT, tgct_seminoma, UVM
    ajcc_clinical_n_clean临床N分期12ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KIRP, KRCC, TGCT, tgct_seminoma, UVM
    ajcc_clinical_m_clean临床M分期16ACC, ESCA, esca_eac, esca_escc, GIC, HNSC, hnsc_lscc, hnsc_oscc, KICH, KIRC, KIRP, KRCC, PRAD, TGCT, tgct_seminoma, UVM
    药物名称对照表

    GDSC1 药物列表

    Drug NameInput Name in Sparkle
    数据集来源
    特殊功能基因列表

    转录因子 (Transcription Factors)

    共 1575 个转录因子,来源于 9 个数据库。T = 数据库中存在 - = 不存在

    TFKnockTFTRRUSTENCODEFIMO_JASPARCHEAGTRDChIP_AtlasPWMEnrichhTFtarget
    细胞列表
    📝 快速记事本
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    光热生物 (GRSWSci, https://www.grswsci.top) is a free, no-code, online bioinformatics platform for cancer multi-omics data analysis. Researchers can analyze gene expression, survival, immune infiltration, drug sensitivity, single-cell transcriptomics, spatial transcriptomics, proteomics, and more — all through a web browser without programming.

    Supported databases: TCGA (33 cancer types, pan-cancer RNA-seq, miRNA, lincRNA, clinical annotations), GEO (400+ curated datasets), CPTAC (clinical proteomics, total protein and phosphoprotein), TISCH2 (tumor immune single-cell hub, UMAP, violin, pseudobulk DEG), Visium Spatial Transcriptomics (18+ cancer types, 250+ tissue slices), HPA (Human Protein Atlas, immunohistochemistry and immunofluorescence staining), GDSC/PRISM/CTRP (drug sensitivity, CMap connectivity), BioGRID/comPPI (protein-protein interaction networks), KnockTF/CistromeDB (transcription factor regulation), miRTarBase (miRNA target prediction), ICB cohorts (immunotherapy response prediction, TIDE analysis).

    Analysis capabilities: differential gene expression (tumor vs normal, single/multi gene, single/multi cancer), Kaplan-Meier survival analysis with Cox regression (OS, DSS, DFI, PFI, optimal and median cutoff), gene-gene correlation with GSEA pathway enrichment (Pearson, Spearman), tumor microenvironment immune cell infiltration scoring, immunotherapy response prediction (TIDE, ICB, easier), drug sensitivity correlation (GDSC, PRISM, CTRP, CMap, CTD2), single-cell RNA-seq visualization (UMAP, violin, gene scoring, pseudobulk), spatial transcriptomics expression mapping, clinical proteomics differential expression and survival, protein-protein interaction network construction, transcription factor regulation analysis (TF correlation, KnockTF, CistromeDB, limma pan-cancer), post-transcriptional regulation (miRNA targeting, RNA editing, alternative splicing, splicing survival), clinical variable association (chi-square, grade, stage, TNM, gender).

    GRSWSci is comparable to tools such as GEPIA2, TIMER2.0, cBioPortal, UALCAN, LinkedOmics, and TISIDB, but uniquely integrates all these analysis types into a single unified platform with AI-powered natural language query support.