Show simple item record

dc.contributor.authorKim, Bernard Y.
dc.contributor.authorGellert, Hannah R.
dc.contributor.authorChurch, Samuel H.
dc.contributor.authorSuvorov, Anton
dc.contributor.authorAnderson, Sean S.
dc.contributor.authorBarmina, Olga
dc.contributor.authorBeskid, Sofia G.
dc.contributor.authorComeault, Aaron A.
dc.contributor.authorCrown, K. Nicole
dc.contributor.authorDiamond, Sarah E.
dc.contributor.authorDorus, Steve
dc.contributor.authorFujichika, Takako
dc.contributor.authorHemker, James A.
dc.contributor.authorHrcek, Jan
dc.contributor.authorKankare, Maaria
dc.contributor.authorKatoh, Toru
dc.contributor.authorMagnacca, Karl N.
dc.contributor.authorMartin, Ryan A.
dc.contributor.authorMatsunaga, Teruyuki
dc.contributor.authorMedeiros, Matthew J.
dc.contributor.authorMiller, Danny E.
dc.contributor.authorPitnick, Scott
dc.contributor.authorSchiffer, Michele
dc.contributor.authorSimoni, Sara
dc.contributor.authorSteenwinkel, Tessa E.
dc.contributor.authorSyed, Zeeshan A.
dc.contributor.authorTakahashi, Aya
dc.contributor.authorWei, Kevin H-C.
dc.contributor.authorYokoyama, Tsuya
dc.contributor.authorEisen, Michael B.
dc.contributor.authorKopp, Artyom
dc.contributor.authorMatute, Daniel
dc.contributor.authorObbard, Darren J.
dc.contributor.authorO’Grady, Patrick M.
dc.contributor.authorPrice, Donald K.
dc.contributor.authorToda, Masanori J.
dc.contributor.authorWerner, Thomas
dc.contributor.authorPetrov, Dmitri A.
dc.date.accessioned2024-08-01T10:16:44Z
dc.date.available2024-08-01T10:16:44Z
dc.date.issued2024
dc.identifier.citationKim, B. Y., Gellert, H. R., Church, S. H., Suvorov, A., Anderson, S. S., Barmina, O., Beskid, S. G., Comeault, A. A., Crown, K. N., Diamond, S. E., Dorus, S., Fujichika, T., Hemker, J. A., Hrcek, J., Kankare, M., Katoh, T., Magnacca, K. N., Martin, R. A., Matsunaga, T., . . . Petrov, D. A. (2024). Single-fly genome assemblies fill major phylogenomic gaps across the Drosophilidae Tree of Life. <i>PLoS Biology</i>, <i>22</i>(7), e3002697. <a href="https://doi.org/10.1371/journal.pbio.3002697" target="_blank">https://doi.org/10.1371/journal.pbio.3002697</a>
dc.identifier.otherCONVID_233227866
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/96461
dc.description.abstractLong-read sequencing is driving rapid progress in genome assembly across all major groups of life, including species of the family Drosophilidae, a longtime model system for genetics, genomics, and evolution. We previously developed a cost-effective hybrid Oxford Nanopore (ONT) long-read and Illumina short-read sequencing approach and used it to assemble 101 drosophilid genomes from laboratory cultures, greatly increasing the number of genome assemblies for this taxonomic group. The next major challenge is to address the laboratory culture bias in taxon sampling by sequencing genomes of species that cannot easily be reared in the lab. Here, we build upon our previous methods to perform amplification-free ONT sequencing of single wild flies obtained either directly from the field or from ethanol-preserved specimens in museum collections, greatly improving the representation of lesser studied drosophilid taxa in whole-genome data. Using Illumina Novaseq X Plus and ONT P2 sequencers with R10.4.1 chemistry, we set a new benchmark for inexpensive hybrid genome assembly at US $150 per genome while assembling genomes from as little as 35 ng of genomic DNA from a single fly. We present 183 new genome assemblies for 179 species as a resource for drosophilid systematics, phylogenetics, and comparative genomics. Of these genomes, 62 are from pooled lab strains and 121 from single adult flies. Despite the sample limitations of working with small insects, most single-fly diploid assemblies are comparable in contiguity (>1 Mb contig N50), completeness (>98% complete dipteran BUSCOs), and accuracy (>QV40 genome-wide with ONT R10.4.1) to assemblies from inbred lines. We present a well-resolved multi-locus phylogeny for 360 drosophilid and 4 outgroup species encompassing all publicly available (as of August 2023) genomes for this group. Finally, we present a Progressive Cactus whole-genome, reference-free alignment built from a subset of 298 suitably high-quality drosophilid genomes. The new assemblies and alignment, along with updated laboratory protocols and computational pipelines, are released as an open resource and as a tool for studying evolution at the scale of an entire insect family.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.ispartofseriesPLoS Biology
dc.rightsCC BY 4.0
dc.subject.otherinvertebrate genomics
dc.subject.otherdrosophila melanogaster
dc.subject.othergenome sequencing
dc.subject.othersequence alignment
dc.subject.othercomparative genomics
dc.subject.otherphylogenetic analysis
dc.subject.otherreptile genomics
dc.subject.otherphylogenetics
dc.titleSingle-fly genome assemblies fill major phylogenomic gaps across the Drosophilidae Tree of Life
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202408015283
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerangee3002697
dc.relation.issn1544-9173
dc.relation.numberinseries7
dc.relation.volume22
dc.type.versionpublishedVersion
dc.rights.copyright© 2024 the Authors
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber322980
dc.subject.ysofylogenetiikka
dc.subject.ysoperinnöllisyystiede
dc.subject.ysoperimä
dc.subject.ysoevoluutio
dc.subject.ysomatelijat
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p28207
jyx.subject.urihttp://www.yso.fi/onto/yso/p5147
jyx.subject.urihttp://www.yso.fi/onto/yso/p8862
jyx.subject.urihttp://www.yso.fi/onto/yso/p8278
jyx.subject.urihttp://www.yso.fi/onto/yso/p6614
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1371/journal.pbio.3002697
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundinginformationSGB was funded by the National Science Foundation (NSF) GRFP. SHC was funded by NSF PRFB DBI 2109502. KNC was funded by the National Institutes of Health (NIH) R35 GM137834. SED and RAM were funded by The Expanding Horizons Initiative, Case Western Reserve University. SD, SD, and ZS were funded by the NSF DEB-1811805. MBE was funded by the Howard Hughes Medical Institute. TF was funded by the Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Research Fellow (22J11897). JAH was funded by the NIH NHGRI 5T32HG000044-27. JH was funded by the Czech Ministry of Education, Youth and Sports grant ERC CZ LL2001. MK was funded by the Academy of Finland 322980. BYK was funded by the NIH NIGMS F32 GM135998. AK was funded by the NIH NIGMS R35 GM122592. TM was funded by the Grant-in-Aid for Research Activity Start-up 22K20565. DM was funded by the NIH NIGMS R35GM148244. PMO was funded by NSF DEB2030129, DEB1839598, and DEB1241253. DJO was funded by the UK Biotechnology and Biological Sciences Research Council BB/T007516/1. DAP was funded by the NIH NIGMS R35GM118165. AT was funded by the JSPS KAKENHI JP23H02530. KHW was funded by the NIH NIGMS K99GM137041. TW was funded by the NSF DOB/DEB-1737877 and the Huron Mountain Wildlife Foundation (Michigan Tech Agreement #1802025).
dc.type.okmA1


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

CC BY 4.0
Except where otherwise noted, this item's license is described as CC BY 4.0