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SRX6262256: Trace experiment for center WUGSC, GENOMIC, species HOMO SAPIENS 2340144417
1 CAPILLARY (AB 310 Genetic Analyzer) run: 51,156 spots, 32.5M bases, 1.8Gb downloads

Design: N/A
Submitted by: WUGSC
Study: Human Genome Structural Variation Project.
show Abstracthide Abstract
The sequence-based survey of human genome structural variation aims to characterize common structural variants that are larger than SNPs, for example, multi-base insertions/deletions, inversions, translocations, and duplications. The approach entails sequencing the ends of genomic libraries from multiple individuals. Discordant end-sequence placements (ESP) against the reference genome are used to create a map of structural variation and to sequence at the level of single basepair resolution the clone corresponding to the variant. The ESP strategy can be efficiently scaled with current technology and is complementary to efforts to obtain human structural variation information by other technologies.
Sample:
SAMN12121739 • SRS5014190 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 2340144417
Instrument: AB 310 Genetic Analyzer
Strategy: CLONEEND
Source: GENOMIC
Selection: unspecified
Layout: SINGLE
Runs: 1 run, 51,156 spots, 32.5M bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR949638051,15632.5M1.8Gb2020-12-05

ID:
8317030

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