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A Unique mutator phenotype reveals complementary oncogenic lesions leading to acute leukemia

NIAID Data Ecosystem2026-04-25 收录

癌症基因组数据

拷贝数变异

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP229816 数据链接链接失效反馈

官方服务：

资源简介：

Sparse Whole Genome Sequencing for Somatic Copy Number Quantification

应用场景：

创建时间：

2019-11-15

癌症基因组数据

差异表达基因分析

Performed using data from The Cancer Genome Atlas, listed in order of log2 fold change. The top 10 upregulated and downregulated genes are shown. Log2 FC, log2 fold-change in gene expression for USC G

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HCC1143.dSKY.svg

乳腺癌基因

拷贝数变异

D.SKY plot show the somatic copy number alterations (sCNAs) in cancer cell-line. For this breast cancer cell-line HCC1143, the D.SKY clearly showed the loss of chr8p and gain of chr8q, a pattern recur

DataCite Commons2020-09-04 更新20

Raw_data.zip

癌症基因组数据

细胞焦亡机制

Comprehensive genomic signature of pyroptosis-related genes and relevant characterization in hepatocellular carcinoma

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Examples of cancer gene mutation orders with a predicted probability greater than random chance.

癌症基因组数据

基因突变预测

The examples in the table are selected based on that the genes have a mutant frequency greater than 40 in the COSMIC database to show the estimation for the common cases. Due to the limited space, the

Figshare2015-12-02 更新30

DataSheet_1_Genetic testing and prognosis of sarcomatoid hepatocellular carcinoma patients.zip

癌症基因组数据

精准医疗

BackgroundSarcomatoid hepatocellular carcinoma (SHC) is a rare epithelial malignancy with high invasiveness and poor prognosis. However, the molecular characteristics and main driver genes for SHC hav

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A Unique mutator phenotype reveals complementary oncogenic lesions leading to acute leukemia

资源简介：

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