PacBio CLR reads were mapped to the HC1-N genome using NGMLR under default settings. SV calling was performed using Sniffles with minimum support at 2 (-s) and minimum length at 30 (-l). We filtered t

NIAID Data Ecosystem90

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

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

Detection of copy number variations in rice using array-based comparative genomic hybridization

水稻拷贝数变异

基因组结构变异检测

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

Exonisation_GB

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