Description of genomic events.

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anTot = nA + nB, where nA and nB represent calculated copy numbers for the separate alleles at a given probe.

创建时间：

2012-12-07

A High-Resolution Map of Segmental DNA Copy Number Variation in the Mouse Genome

Submicroscopic (less than 2 Mb) segmental DNA copy number changes are a recently recognized source of genetic variability between individuals. The biological consequences of copy number variants (CNVs

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Supplementary Material for: Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human

At present, low-pass whole-genome sequencing (WGS) is frequently used in clinical research and in the screening of copy number variations (CNVs). However, there are still some challenges in the detect

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CEL file for isolate IC313

aCGH raw data submitted to Gene Expression Omnibus

DataONE2015-03-18 更新70

Additional file 8 of A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing

Additional file 8: Table S6. Functional enrichment of KEGG analysis of CNVR-harbored genes.

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Additional file 8 of An initial comparative map of copy number variations in the goat (Capra hircus) genome

Additional file 8:Gene Ontology (GO) annotation of genes included in goat CNVRs. Ensembl cattle transcripts located in goat CNVRs have been annotated using GO for Biological process, Cellular componen

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