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Zebrafish genome assemblies
The integrated zebrafish genome assembly is created by filling the remaining gaps in the clone path with whole genome shotgun (WGS) contigs.The most recent whole genome shotgun assembly, WGS31, has been created using Illumina sequencing reads from a double-haploid Tübingen fish (289 million reads providing approximately 30-fold coverage), combined with capillary sequencing reads from a second related double-haploid Tuebingen fish (12.2 million reads providing approximately 7.5-fold coverage). This use of data from double-haploid Tuebingen fish results in less artificial haplotypic duplication than was found in previous WGS assemblies which were generated from multiple individual diploid fish. A novel de Bruijn graph based algorithm called Fuzzypath was used to assemble the Illumina reads into short sequence contigs; these contigs were then combined with the capillary reads using the Phusion assembler.
Earlier WGS assemblies were based on DNA sequence from ~1000 zebrafish embryos. The resulting reads were assembled with Phusion. From Zv5 onwards, WGS assemblies included reads from a single Tübingen, double haploid zebrafish.
Pre-ensemblPre-ensembl currently features the most recent assembly, Zv9. EnsemblEnsembl currently features the previous Zv8 assembly complete with gene build and comparative genomics data. DAS sources can be added to the browser to view additional data aligned to the genome
Previous assemblies
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