Copy number variations (CNVs) can create new genes, change gene dosage, reshape gene structures, and modify elements regulating gene expression. As with all types of genetic variation, CNVs may influe

NIAID Data Ecosystem90

Ruler Arrays Reveal Haploid Genomic Structural Variation

基因组结构变异检测

基因单倍型分析

Despite the known relevance of genomic structural variants to pathogen behavior, cancer, development, and evolution, certain repeat based structural variants may evade detection by existing high-throu

NIAID Data Ecosystem20

Escherichia coli Long-term Evolution Experiment 500 and 1000 Generation Population Sequencing. Escherichia coli REL606

微生物进化基因组学

基因组结构变异检测

New mutations leading to structural variation (SV) in genomes — in the form of mobile element insertions, large deletions, gene duplications, and other chromosomal rearrangements — can play a key role

NIAID Data Ecosystem100

Summary of all DNA sequence rearrangements identified.

基因组结构变异检测

基因组重测序分析

The table shows for each sample the number of read pairs in unusual configuration indicating putative DNA sequence rearrangements. Dashes (-) indicate that no read pairs supported a sequence rearrange

NIAID Data Ecosystem70

De novo structural variants (insertions and deletions) primary

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