<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR181/057/SRR18100457/SRR18100457_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR181/056/SRR18100456/SRR18100456_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR181/057/SRR18100457/SRR18100457_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR181/056/SRR18100456/SRR18100456_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>University of Kansas</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA809365</full_dataset_link><long_description>Isolated samples of nematocyst-enriched bulk sequencing and non-nematocyst bulk sequencing. These samples were obtained from FACS samples derived from a newly established minicollagen-1 (nematocyst-specific)) reporter line for Hydractinia symbiolongicarpus. The goal of this project was to determine putative venom-like genes from Hydractinia via a nematocyst-enriched de novo transcriptome assembly.</long_description><tag>xref:EuropePMC:PMC8917316</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>Hydractinia nematocyst-specific sequencing</description><dates><last_updated>2023-05-19</last_updated><first_public>2022-03-09</first_public></dates><accession>PRJNA809365</accession><cross_references/></HashMap>