Illumina sequencing of library 10756929, constructed from sample accession ERS499134 for study accession ERP006133.  This is part of an Illumina multiplexed sequencing run (13466_1).  This submission includes reads tagged with the sequence GCAACATT.

Illumina HiSeq 2500 paired end sequencing

3' end enriched mRNA from single genotyped homozygous mutant embryo for dnmt8, allele sa3105,ZMP phenotype 87 clutch 1. A 8 base indexing sequence (GCAACATT) is bases 13 to 20 of read 1 followed by CG and polyT.  More information describing the mutant phenotype can be found at the Wellcome Trust Sanger Institute Zebrafish Mutation Project website http://www.sanger.ac.uk/cgi-bin/Projects/D_rerio/zmp/search.pl?q=zmp_ph87

Danio rerio

Paired-end sequence data from the IlluminaHiSeq was prepared for zebrafish embryos genotyped for one or more alleles involved in DNA methylation and demethylation identified by the Zebrafish Mutation Project.

Total RNA was extracted from zebrafish embryos genotyped for one or more alleles in genes involved in DNA methylation and demethylation identified by the Zebrafish Mutation Project (http://www.sanger.ac.uk/Projects/D_rerio/zmp/). The 3' end of fragmented RNA was pulled down using polyT oligos attached to magnetic beads, reverse transcribed, made into Illumina libraries and sequenced using IlluminaHiSeq paired-end sequencing. Protocol: Total RNA was extracted and DNase treated. Fragmented RNA was enriched for the 3’ ends by pull down using a  polyT oligo attached to magnetic beads. An RNA oligo comprising part of the Illumina adapter 2 was ligated to the 5’ end of the captured RNA and the RNA was eluted from the beads. Reverse transcription was primed with an anchored polyT oligo with part of Illumina adapter 1 at the 5’ end followed by 12 random bases, then an 8 base indexing tag, then CG and 14 T bases. An Illumina library with full adapter sequence was produced by 20 cycles of PCR. 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/

Transcriptome_profiling_of_embryos_genotyped_for_one_or_more_alleles_in_genes_involved_in_DNA_methylation_and_demethylation_identified_by_the_Zebrafish_mutation_project

Transcriptome_profiling_of_embryos_genotyped_for_one_or_more_alleles_in_genes_involved_in_DNA_methylation_and_demethylation_identified_by_the_Zebrafish_mutation_project

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