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ERX1413368: HiSeq X Ten paired end sequencing
1 ILLUMINA (HiSeq X Ten) run: 513.8M spots, 155.2G bases, 38.9Gb downloads

Submitted by: Broad Institute (BROAD INSTITUTE)
Study: Evaluating variant calling accuracy with CHM1 and CHM13 haploid data
show Abstracthide Abstract
CHM1 and CHM13 are haploid human cell lines. This study sequenced the two cell lines on HiSeq-X10 with the standard protocol at Broad Institute, and sequenced a pseudo-diploid sample by experimentally mixing CHM1 and CHM13 DNA at approximately 50-50%. Incorporating public CHM1 and CHM13, including whole-genome PacBio assemblies for each cell line, this study aims to construct a comprehensive truth data set and data resource for evaluating and improving small and structural variant calling accuracy. Note: please contact the submitters if you want to use this data set in a publication.
Sample: Mixed CHM1 and CHM13
SAMEA3911976 • ERS1099110 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Pond-487422
Instrument: HiSeq X Ten
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: PCR-free
Runs: 1 run, 513.8M spots, 155.2G bases, 38.9Gb
Run# of Spots# of BasesSizePublished
ERR1341796513,796,566155.2G38.9Gb2016-04-02

ID:
2403896

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