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ERX4753342: NextSeq 500 paired end sequencing
1 ILLUMINA (NextSeq 500) run: 756,750 spots, 121.1M bases, 46.8Mb downloads

Design: Paired-End Sequencing
Submitted by: EUROPEAN MOLECUALR BIOLOGY LABORATORY, GENOME BIOLOGY UNIT (EUROPEAN MOLECUALR BIOLOGY LABORATORY, GENOME BIOL)
Study: Strand-seq data of HGSVC samples
PRJEB39750 • ERP123307 • All experiments • All runs
show Abstracthide Abstract
Strand-seq (single-cell and single-strand sequencing) libraries were generated for human lymphoblastic cell lines (LCL) to produce haplotype-informative data for select human genomes as part of the HGSVC (Human Genome Structural Variation Consortium) project - phase 2.
Sample: Coriell GM18534
SAMN00000419 • SRS000649 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GM18534_PE20388
Instrument: NextSeq 500
Strategy: WGS
Source: GENOMIC
Selection: MNase
Layout: PAIRED
Construction protocol: Strand-Seq
Runs: 1 run, 756,750 spots, 121.1M bases, 46.8Mb
Run# of Spots# of BasesSizePublished
ERR4884405756,750121.1M46.8Mb2020-12-11

ID:
12642310

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