官方服务：
资源简介：
Whole genome and whole exome of esophageal cancer
应用场景：
创建时间：
2013-12-17
相关数据集
97dd9532-0482-4bf1-ad1d-fb976b8ed7ea - samples
This dataset contains whole-genome sequencing data files from colon organoid cultures, which were mutated using CRISPR-Cas9 for specific genes (APC, KRAS, TP53 and SMAD4) to generate in vitro transfor
NIAID Data Ecosystem70
Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion
The hypothesis that chromosomal fragile sites may be “weak links” that result in hot spots for cancer-specific chromosome rearrangements was supported by the discovery that numerous cancer cell homozy
PubMed Central1997-12-23 更新30
3 cases of renal cell carcinomas with TFEB amplification
We report here 3 cases of a very rare entity of renal cell carcinomas (RCCs) that present an amplification of TFEB gene. This amplification, as well as translocation t(6;11) involving TFEB and MALAT1,
NIAID Data Ecosystem30
Additional file 3 of Integrated genomic and transcriptomic analysis revealed mutation patterns of de-differentiated liposarcoma and leiomyosarcoma
Additional file 3: Supplementary Table S3. LMS_amplified_gene list in 0.95 confidence level
DataCite Commons2024-02-07 更新50
Supplementary Table 3 from Tumor Suppressor Genes with Segmental Duplications Are Prone to Somatic Deletions and Structural Variations
Results of Fisher's exact tests comparing the number of SDs association with oncogenes and tumor suppressor genes (TSGs) against non-cancer genes across multiple species.
NIAID Data Ecosystem30
