<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><technology_type>Illumina MiSeq</technology_type><study_type>Resequencing</study_type><full_dataset_link>https://ega-archive.org/studies/EGAS00001000437</full_dataset_link><host>EGA</host><description>EGA study EGAS00001000437</description><dataset_title>Deep sequencing of S7EPC genome</dataset_title><repository>EGA</repository><category>restricted</category><name_synonyms>whole genome, Genomes.</name_synonyms><description_synonyms>PRE, INO1, Anchored Polymerase Chain Reaction, ichthyosis-prematurity syndrome, human being, PhrB photolyase activity, IPS, Modern, deoxyribonucleic cyclobutane dipyrimidine photolyase activity, ino1-B, Polymerase Chain Reactions, photoreactivating enzyme activity, Inverse, IPS-1, pigmented epithelium, Cell, gDNA, Human, Publication., Inverse PCR, MODIFIER OF SNC1, Homo sapiens, retinal pigment, Publication, ips, ichthyosis congenita 4, deoxyribonucleic photolyase activity, dipyrimidine photolyase (photosensitive), 3, stratum pigmentosa retinae, NUP96, Polymerase Chain, ino1, IPS 1, epithelium, Man, Library, retinal pigment layer, PCR, Anchored, MOS3, RPE, deoxyribocyclobutadipyrimidine pyrimidine-lyase activity, Reactions, Nested, Man (Taxonomy), Nested Polymerase Chain Reaction, PRECOCIOUS, library construction, photolyase activity, pigmented retina, Inverse Polymerase Chain Reaction, nucleic acid library construction, F23A5.3, pooled, nucleic acid library preparation, isyna1, ichthyosis congenita IV, human, DNA cyclobutane dipyrimidine photolyase activity, polymerase chain reaction, SUPPRESSOR OF AUXIN RESISTANCE 3, p. pigmentosa retinae, FATP4, phr A photolyase activity, DNA-photoreactivating enzyme, INOS, Reaction, Modern Man, MiSeq, ACSVL4, Nested PCR, deoxyribonucleate pyrimidine dimer lyase (photosensitive), Anchored PCR, ino1-a, inos, F23A5_3</description_synonyms></additional><is_claimable>false</is_claimable><name>Deep sequencing of S7EPC genome</name><description>PCR products were obtained from each target loci using genomic DNA from human iPS cells. Subsequently, PCR products are pooled and subjected to Illumina library preparation.  The library will be sequenced either by HiSeq or MiSeq. 

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/</description><dates><updated>2021-04-23 20:10:07</updated></dates><accession>EGAS00001000437</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAD00001000607</EGA><EGA>EGAC00001000205</EGA></cross_references></HashMap>