<HashMap><database>EVA</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>0</viewCount><searchCount>0</searchCount></scores><additional><dataset_type>Whole Genome Sequencing</dataset_type><omics_type>Genomics</omics_type><submitter>University of Kentucky</submitter><instrument_platform>Illumina HiSeq 2500</instrument_platform><species>Ambystoma 'unisexual Hybrid'</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJEB30506</full_dataset_link><repository>EVA</repository><name_synonyms>Mexican, axolotl, Axolotls, Ambystoma mexicanum (Shaw &amp; Nodder, 1798), mexicanums, Mexican Salamander, Chromosome., Ambystoma, Ambystoma mexicanums, Salamander, Axolotl, Gyrinus mexicanus</name_synonyms><description_synonyms>prophase chromosome, scale tissue, me75, Lr, cou, Chromosome, scale, Genomes, interphase chromosome, plant peltate hair, Bra, Low, chromatid, whole genome, scales, peltate hair., Tl3, Tl2, D17Mit170, T1</description_synonyms><citation_count>0</citation_count></additional><is_claimable>false</is_claimable><name>Scaffolding of Ambystoma mexicanum chromosomes</name><description>Analyses of low coverage sequence data yielded 12.6 million A. mexicanum / A. tigrinum polymorphisms segregating in a meiotic mapping panel. These were distributed across 98,802 scaffolds with individual scaffolds containing between 1 and 12,108 polymorphisms. Segregation patterns were used for meiotic maping and genome scaffoding to achieve chromosome-scale contiguity.</description><dates><publication>2019-01-14</publication></dates><accession>PRJEB30506</accession><cross_references><TAXONOMY>8307</TAXONOMY></cross_references></HashMap>