Highcoverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

dc.article.end-page2073en
dc.article.start-page2061en
dc.citation.doi10.1101/GR.279273.124en
dc.contributor.authorJonas Gustafsonen
dc.contributor.authorSophia Gibsonen
dc.contributor.authorNikhita Damarajuen
dc.contributor.authorMiranda PG Zaluskyen
dc.contributor.authorDavid Twesigomween
dc.contributor.authorE et alen
dc.date.accessioned2025-03-29T10:54:52Z
dc.departmentSYDNEY BRENNER INSTITUTE FOR MOLECULAR BIOSCIENCEen
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationWOSen
dc.identifier.issn1088-9051en
dc.identifier.urihttps://hdl.handle.net/10539/44498
dc.journal.titleHighcoverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variationen
dc.journal.volume34en
dc.publisherCOLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPTen
dc.titleHighcoverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variationen
dc.typeJournal Articleen

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