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ERX13089618: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 2.8M spots, 831M bases, 307.9Mb downloads

Design: Illumina sequencing of library SQPP-59407-L:F1, constructed from sample accession ERS18400162 for study accession ERP000190. This is part of an Illumina multiplexed sequencing run (49507_1). This submission includes reads tagged with the sequence GCTTGTCA.
Submitted by: Wellcome Sanger Institute
Study: MalariaGEN
show Abstracthide Abstract
MalariaGEN aims to bring together malaria genetics with epidemiological information across both time and space. The project has two distinct but complementary goals; to simplify genetic data reporting so that more users are able to analyse and interpret the key features of their data, focusing on what is of most importance for field research and malaria control in a timely manner; and to create an open access global observatory across time and space for genetic variation and other relevant metadata such as malaria prevalence and deployment of control measures. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/.
Sample: 7540STDY14553134
SAMEA115380796 • ERS18400162 • All experiments • All runs
Library:
Name: SQPP-59407-L:F1
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: HiSeqX PCR free
Runs: 1 run, 2.8M spots, 831M bases, 307.9Mb
Run# of Spots# of BasesSizePublished
ERR137195192,751,777831M307.9Mb2024-09-26

ID:
35378260

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