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资源简介：
This project hosts cancer genomic data from the laboratory of Dr. Subhajyoti De.
应用场景：
创建时间：
2019-09-28
相关数据集
Additional file 2 of BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes
Supplementary Table S1. (XLS 24 kb)
DataCite Commons2024-12-16 更新50
DataSheet_2_Association of Pathway Mutations With Survival in Taiwanese Breast Cancers.xlsx
Breast cancer is the most common invasive cancer in women worldwide. Next-generation sequencing (NGS) provides a high-resolution profile of cancer genome. Our study ultimately gives the insight for ge
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DataSheet1_High expression of B4GALT1 is associated with poor prognosis in acute myeloid leukemia.docx
Acute myeloid leukemia is the most prevalent type of leukemia in adults and is prone to relapse and chemoresistance, with a low long-term survival rate. Therefore, the identification of quality biomar
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Table8_RNA-SSNV: A Reliable Somatic Single Nucleotide Variant Identification Framework for Bulk RNA-Seq Data.XLSX
The usage of expressed somatic mutations may have a unique advantage in identifying active cancer driver mutations. However, accurately calling mutations from RNA-seq data is difficult due to confound
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50K SNP Copy Number Analysis of Ovarian Carcinomas. Homo sapiens
Genome-wide copy number variation was measured in primary tumours of the ovary, Fallopian tube and peritoneum. A well-defined subset of advanced-stage serous tumors was then used to relate CNV to prim
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