Info • Jimgerdemannia flammicorona AD002


[October 2018] The genome of Jimgerdemannia flammicorona was sequenced at JGI, but assembled and annotated by Ying Chang at Oregon State University. JGI tools were used to automatically annotate predicted proteins. The material used for sequencing of Jimgerdemannia flammicorona resulted in a metagenome. Therefore, assembly was done using Spades v3.12.0 and VizBin (Laczny et al., 2015) was used to separate individual genomes. Maker was then used to annotate the extracted J. flammicorona AD002 genome. Please note that Ying does not maintain this copy of the genome and therefore it is not automatically updated.

Summary statistics for the Jimgerdemmania flammicorona AD002 v1.0 release are below.
Genome Assembly
Genome Assembly size (Mbp) 231.32
Sequencing read coverage depth
# of contigs 35354
# of scaffolds 35354
# of scaffolds >= 2Kbp 26181
Scaffold N50 6397
Scaffold L50 (Mbp) 0.01
# of gaps 0
% of scaffold length in gaps 0.0%
Three largest Scaffolds (Mbp) 0.09, 0.08, 0.07

Gene Models ExternalModels
length (bp) of: average median
gene 1697 1278
transcript 1289 975
exon 295 182
intron 123 100
protein length (aa) 353 261
exons per gene 4.37 3
# of gene models 13838


Ying Chang, Oregon State University, USA

Joseph Spatafora, Oregon State University, USA

Greg Bonito, Michigan State University, USA

Alessandro Desirò, Michigan State University, USA

Genome Reference(s)


The work conducted by the U.S. Department of Energy Joint Genome Institute, a DOE Office of Science User Facility, is supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.