Homo sapiens alternate pseudohaplotype genome sequencing. Homo sapiens
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PRJNA588278_SAMN14178719_2
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创建时间：
2020-10-29
相关数据集
MOESM1 of Structural variant calling: the long and the short of it
Additional file 1: Table S1.
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Summary of all DNA sequence rearrangements identified.
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
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Additional file 10 of Hidden biases in germline structural variant detection
Additional file 10: Table S9. Distribution of LCL5 singleton SVs across chromosomes for all strategies (mapper, replicate, center, dedup/recal).
Figshare2021-12-20 更新10
Escherichia coli Long-term Evolution Experiment 500 and 1000 Generation Population Sequencing. Escherichia coli REL606
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
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Ruler Arrays Reveal Haploid Genomic Structural Variation
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
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