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ERX12973168: Illumina NovaSeq X paired end sequencing
1 ILLUMINA (Illumina NovaSeq X) run: 426.4M spots, 128.8G bases, 33.4Gb downloads

Design: Illumina sequencing of sample accession SAMEA115109888 for study accession PRJEB79197. This submission includes reads tagged with the sequence GCTCGATT. Library was made using a Hi-C - Arima v2 kit with restriction enzyme motif ^GATC,G^ANTC,C^TNAG,T^TAA.
Submitted by: Wellcome Sanger Institute
Study: Malacosoma alpicolum, genomic and transcriptomic data
show Abstracthide Abstract
This project collects the genomic and transcriptomic data generated for Malacosoma alpicolum. The assembly is provided by the Wellcome Sanger Institute Tree of Life Programme (https://www.sanger.ac.uk/programme/tree-of-life/). The data under this project are made available subject to the Tree of Life Open Data Release Policy (https://www.darwintreeoflife.org/project-resources/).
Sample: 59563-tol
SAMEA115109888 • ERS17745607 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq X
Strategy: Hi-C
Source: GENOMIC
Selection: Restriction Digest
Layout: PAIRED
Construction protocol: Hi-C - Arima v2
Runs: 1 run, 426.4M spots, 128.8G bases, 33.4Gb
Run# of Spots# of BasesSizePublished
ERR13602175426,361,780128.8G33.4Gb2024-08-27

ID:
34908343

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