1:關於真菌基因組次級代謝分析
可以使用SMURF和AntiSMASH,基因組注釋使用MAKER,基因與測使用AUGUSTUS並基於Aspergillus oryzae物種的訓練結果。拼接使用的是VelvetOptimizer,基因功能注釋使用的是interproscan.測序深度27x,N50 為48,518。1,231 contigs。基因組大小為:31,415,732bp。GC含量:48.24% 使用tRNAscan-SE與測tRNA.
2014-Draft Genome Sequence of Penicilliumexpansum Strain R19, Which Causes Postharvest Decay of Apple Fruit
2:關於真菌基因組的分析
在已知近源物種的基礎上,可以分析結構變異
(例如染色體重排等)
2014-Complete Sequencing andChromosome-Scale Genome Assembly of the Industrial Progenitor Strain P2niaD18from the Penicillin Producer Penicillium chrysogenum
3:在真菌基因預測
本文分別使用了Fgenesh(Penicilliumfuniculosum 訓練)與GeneMark- ES(基於自身訓練),基於預測是在大於1Kb的且經過masker重複序列的基礎上進行的將兩者結果整合。關於功能注釋內容包括:nr\interproscan\Swiss-Prot/UniProtKB\GO\kegg(KAAS )
2014-Genome sequencing of high-penicillin producingindustrial strain of Penicillium chrysogenum
4:這篇文章裡關注了水平基因轉移
組裝完基因預測先是使用GeneMark and TWINSCAN分別與測然後再合併,再合併genewise的結果(Genomic sequences with 90% identity that spanned more than 80% of aprotein were ex- tended 500 bp up and downstream and passed to Gene-Wise topredict gene models. )假定基因的功能注釋使用blast2go.假定蛋白的功能域和GO分析可以使用 Agbase
2014-Genome sequencing and analysis of thepaclitaxel-producing endophytic fungus Penicillium aurantiogriseum NRRL 62431
5:細胞色素P450
(cytochromeP450或CYP450,簡稱CYP450)為一類亞鐵血紅素—硫醇鹽蛋白的超家族,它參與內源性物質和包括藥物、環境化合物在內的外源性物質的代謝.網址:http://drnelson.uthsc.edu/P450seqs.dbs.html。使用blastp(e<10-5).(A physical CYP gene cluster was de ned as threeor more CYPs present within a 100-kb sliding window of the genomic sequence orfewer than 10 genes between CYPs a er they had been sorted into groups alongthe chromosomes. If two adjacent clusters overlapped, they were merged to formone larger cluster)
2012-Genome sequence of the model medicinalmushroom Ganoderma lucid
http://drnelson.uthsc.edu/cytochromeP450.html
6:真菌基因組的大小範圍
In fungi, the diversity of genomes varies from 8.97 Mb to 177.57 Mb.
Mohanta T K, Bae H. The diversity of fungalgenome[J]. Biological procedures online, 2015, 17(1)
原文地址:http://blog.sina.com.cn/s/blog_83f77c940102vx0h.html
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