Info • Endogone sp FLAS 59071

Status

[October 2018] The genome of Endogone sp. FLAS 59071 was sequenced at JGI using Illumina, 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 Endogone sp. 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 Endogone sp. FLAS 59071 genome. Please note that Ying does not maintain this copy of the genome and therefore it is not automatically updated.

Summary statistics for the Endogone sp. FLAS 59071 v1.0 release are below.
Genome Assembly
Genome Assembly size (Mbp) 95.55
Sequencing read coverage depth
# of contigs 15409
# of scaffolds 15409
# of scaffolds >= 2Kbp 10610
Scaffold N50 2370
Scaffold L50 (Mbp) 0.01
# of gaps 0
% of scaffold length in gaps 0.0%
Three largest Scaffolds (Mbp) 0.11, 0.10, 0.09


Gene Models ExternalModels
length (bp) of: average median
gene 2039 1565
transcript 1544 1194
exon 305 179
intron 124 103
description:
protein length (aa) 413 313
exons per gene 5.07 4
# of gene models 9569


Collaborators

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)

Please cite the following publication(s) if you use the data from this genome in your research:

Chang Y, Desirò A, Na H, Sandor L, Lipzen A, Clum A, Barry K, Grigoriev IV, Martin FM, Stajich JE, Smith ME, Bonito G, Spatafora JW
Phylogenomics of Endogonaceae and evolution of mycorrhizas within Mucoromycota.
New Phytol. 2019 Apr;222(1):511-525. doi: 10.1111/nph.15613

Funding

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.