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资源简介：
DNA CNV of 63 paired Cancer-Control for 22 chromosomes.
应用场景：
创建时间：
2024-04-14
相关数据集
Additional file 14: Figure S5. of A systematic comparison of copy number alterations in four types of female cancer
A schematic view of two common genes among female cancers. This schematic view shows the genomic positions of two genes that were found common among female cancers. The figure further suggests an expl
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Additional file 5 of Hierarchical discovery of large-scale and focal copy number alterations in low-coverage cancer genomes
Additional file 5. Supplementary Table S4
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Raw read counts and phased SNP counts for every single cell in the sequencing datasets of the breast cancer patient S0 from "Characterizing allele- and haplotype-specific copy numbers in single cells with CHISEL"
This dataset contains the raw read counts and phased SNP counts for every single cell in the sequencing datasets of breast cancer patient S0 from “Characterizing allele- and haplotype-specific copy nu
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Functional Copy-Number Alterations in Cancer
Understanding the molecular basis of cancer requires characterization of its genetic defects. DNA microarray technologies can provide detailed raw data about chromosomal aberrations in tumor samples.
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