数据链接：
官方服务：
资源简介：
Infile and output from BayeScan analyses. Also included is a file associating SNPs with their locus names.
应用场景：
创建时间：
2015-06-02
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
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
NIAID Data Ecosystem30
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
NIAID Data Ecosystem10
Data_Sheet_1_Genomic Positional Dissection of RNA Editomes in Tumor and Normal Samples.ZIP
RNA editing is phenomenon that occurs in both protein coding and non-coding RNAs. Increasing evidence have shown that adenosine-to-inosine RNA editing can potentially rendering substantial functional
NIAID Data Ecosystem40
The Mutational Landscape of Lethal Castrate Resistant Prostate Cancer. Homo sapiens
Characterization of the prostate cancer transcriptome and genome has identified chromosomal rearrangements and copy number gains/losses, including ETS gene fusions, PTEN loss and androgen receptor (AR
NIAID Data Ecosystem20
