Author
BOWERS, ROBERT - Joint Genome Institute | |
KYRPIDES, NIKOS - Joint Genome Institute | |
STEPANAUSKAS, RAMUNAS - Bigelow Laboratory For Ocean Sciences | |
HARMON-SMITH, MIRANDA - Joint Genome Institute | |
SCHULZ, FREDERIK - Joint Genome Institute | |
DOUD, DEVIN - Joint Genome Institute | |
REDDY, T.B. - Joint Genome Institute | |
JARETT, JESSICA - Joint Genome Institute | |
Rivers, Adam | |
ELOE-FADROSH, EMILEY - Joint Genome Institute | |
TRINGE, SUSANNAH - Joint Genome Institute | |
IVANOVA, NATALIA - Joint Genome Institute | |
COPELAND, ALEX - Joint Genome Institute | |
CLUM, ALICIA - Joint Genome Institute | |
BECRAFT, ERIC - Bigelow Laboratory For Ocean Sciences | |
MALMSTROM, REX - Joint Genome Institute | |
BIRREN, BRUCE - Broad Institute Of Mit/harvard | |
SCHRIML, LYNN - National Cancer Institute (NCI, NIH) | |
PODAR, MIRCEA - Oak Ridge National Laboratory | |
BORK, PEER - European Molecular Biology Laboratory | |
WEINSTOCK, GEORGE - National Center For Agriculture And Forestry Technologies (CENTA) | |
BANFIELD, JILLIAN - University Of California | |
GARRITY, GEROGE - Michigan State University | |
HUGENHOLTZ, PHILIP - University Of Queensland | |
PARKS, DONOVAN - University Of Queensland | |
TYSON, GENE - University Of Queensland | |
RINKE, CHRISTIAN - University Of Queensland | |
DODSWORTH, JEREMY - California State University | |
YOOSEPH, SHIBU - University Of Queensland | |
SUTTON, GRANGER - J Craig Venter Institute | |
YILMAZ, PELIN - Max Planck Society | |
GLÖCKNER, FRANK - Max Planck Society | |
MEYER, FOLKER - University Of Chicago | |
GILBERT, JACK - University Of Chicago | |
NELSON, WILLIAM - Pacific Northwest National Laboratory | |
HALLAM, STEVEN - University Of British Columbia | |
JUNGBLUTH, SEAN - Energy Joint Genome Institute | |
ETTEMA, THIJS - Uppsala University | |
TIGHE, SCOTT - University Of Vermont | |
KONSTANTINIDIS, KONSTANTINOS - Georgia Institute Of Technology | |
LIU, WEN-TSO - University Of Illinois | |
BAKER, BRETT - University Of Texas At Austin | |
RATTEI, THOMAS - University Of Vienna | |
EISEN, JONATHAN - University Of California | |
HEDLUND, BRIAN - University Of Nevada Las Vegas, Las Vegas, Nv | |
MCMAHON, KATHERINE - University Of Wisconsin | |
FIERER, NOAH - University Of Colorado | |
KNIGHT, ROB - University Of California | |
FINN, ROB - European Bioinformatics Institute | |
KARSCH-MIZRACHI, ILENE - National Institutes Of Health (NIH) | |
EREN, A - University Of Chicago | |
WOYKE, TANJA - Energy Joint Genome Institute |
Submitted to: Nature Biotechnology
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 7/27/2017 Publication Date: 8/8/2017 Publication URL: https://handle.nal.usda.gov/10113/5801851 Citation: Bowers, R.M., Kyrpides, N.C., Stepanauskas, R., Harmon-Smith, M., Schulz, F., Doud, D., Reddy, T.K., Jarett, J., Rivers, A.R., Eloe-Fadrosh, E.A., Tringe, S.G., Ivanova, N., Copeland, A., Clum, A., Becraft, E.D., Malmstrom, R.R., Birren, B., Schriml, L., Podar, M., Bork, P., Weinstock, G.W., Banfield, .F., Garrity, G.M., Hugenholtz, P., Parks, D.H., Tyson, G.W., Rinke, C., Dodsworth, J.A., Yooseph, S., Sutton, G., Yilmaz, P., Glöckner, F.O., Meyer, F., Gilbert, J.A., Nelson, W.C., Hallam, S.J., Jungbluth, S.P., Ettema, T.J., Tighe, S., Konstantinidis, K.T., Liu, W., Baker, B.J., Rattei, T., Eisen, J.A., Hedlund, B., Mcmahon, K.D., Fierer, N., Knight, R., Finn, R., Karsch-Mizrachi, I., Eren, A.M., Woyke, T. 2017. Minimum information about a single amplified genome (MISAG) and a metagenome-assembled genome (MIMAG) of bacteria and archaea. Nature Biotechnology. 35, 725–731. doi:10.1038/nbt.3893. Interpretive Summary: Most microorganisms cannot be grown in the laboratory. Having the genome of these organisms would reveal their role in the environment, but conventional genome sequencing requires growth in the laboratory. To sequence the genomes on these uncultivated organisms two alternative methods are used: singe cell sequencing and metagenome sequencing followed by the computational construction of “metagenome assembled genomes”. Because of the technical challenges of doing this, these genomes are often missing some components and the quality can vary greatly. This paper puts forth official Genomic Standards Consortium standards for what constitutes a Finished, High Quality Draft, Medium Quality Draft or Low Quality Draft single cell genome or metagenome assembled genome. This standardization is important because it will allow scientists to rapidly compare their data to other genomes derived from single cells or metagenomes. Technical Abstract: We present two standards developed by the Genomic Standards Consortium (GSC) for reporting bacterial and archaeal genome sequences. Both are extensions of the minimum information about any (x) sequence (MIxS). The standards are the minimum information about a single amplified genome (MISAG) and the minimum information about a metagenome-assembled genome (MIMAG), including (but not limited to) assembly quality, and estimates of genome completeness and contamination. These standards can be used in combination with other GSC checklists including the minimum information about a genome sequence (MIGS), minimum information about a metagenomic sequence (MIMS) and minimum information about a marker gene sequence (MIMARKS). Community-wide adoption of MISAG and MIMAG will facilitate more robust comparative genomic analyses of bacterial and archaeal diversity. |