官方服务:
资源简介:
CNVs detected in MMC-treated and untreated cells using molecular karyotyping. Raw data
应用场景:
创建时间:
2021-12-29
相关数据集
Additional file 1: Table S1. of A systematic comparison of copy number alterations in four types of female cancer
Additional clinical data for the Breast and Ovarian cohort. A summary of the clinicopathological characteristics for the breast and ovarian cohorts is available (XLSX 102 kb)
DataCite Commons2024-12-13 更新130
Additional file 5 of MetaCNV - a consensus approach to infer accurate copy numbers from low coverage data
Additional file 5. CNVcalling MCF7 CNV calling results for MCF7.
DataCite Commons2020-08-25 更新90
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]. Homo sapiens
Background: High-resolution microarray technology is routinely used in basic research and clinical practice to efficiently detect copy number variants (CNVs) across the entire human genome. A new gene
NIAID Data Ecosystem70
Next generation sequencing reveals the diversity and population-genetic properties of cattle CNVs. Bos taurus
Structural and functional impacts of copy number variations (CNVs) on livestock genomes are not yet well understood. In this study, we have identified 1853 CNV regions (CNVRs) using population-scale s
NIAID Data Ecosystem90
Single-Cell Whole Genome Analyses by Linear Amplification via Transposon Insertion (LIANTI)
Single-cell genomics is important for biology and medicine. However, current whole genome amplification (WGA) methods are limited by low accuracy of copy number variation (CNV) detection and low ampli
DataCite Commons2020-10-10 更新90



