ライフサイエンスコーパス: fungal genome

1 at Fsmapk is present as a single copy in the fungal genome.

2 earrangements (CRs) are widely documented in fungal genomes.

3 egradation" (i.e., antibiotic resistance) in fungal genomes.

4 rotrophs, which we analyzed along with other fungal genomes.

5 ined in a rapidly evolving region of diverse fungal genomes.

6 ns, based on annotations from proteins in 46 fungal genomes.

7 rces driving the diversification of GH28s in fungal genomes.

8 n 2, that identifies protein-coding genes in fungal genomes.

9 markable increase in the number of sequenced fungal genomes.

10 ses found in a variety of plant, animal, and fungal genomes.

11 ching, analysing and visualizing features of fungal genomes.

12 ge DNA inserts (up to 230 kb) into plant and fungal genomes.

13 integrating large DNA inserts into plant and fungal genomes.

14 Comparative analyses of 31 fungal genomes (12 generated for this study) suggest tha

15 Here, the increasing number of sequenced fungal genomes allowed for systematic identification of

16 SMs are found in contiguous gene clusters in fungal genomes, an atypical arrangement for metabolic pa

17 The complexity of the fungal genome and lifestyle questions the existence of o

18 e a complete toolset, including an annotated fungal genome and methods for genetic manipulation of th

19 includes over 23 000 bacterial genomes, 400 fungal genomes and 100 protist genomes, in addition to 5

20 query to search their counterparts in other fungal genomes and found that the secretome profiles clu

21 We provide here an overview of available fungal genomes and highlight some of the biological insi

22 es exist in all Ascomycete and Basidiomycete fungal genomes and that all possess an SH3 domain and a

23 enzymes for polysaccharide deconstruction in fungal genomes and will help identify new strains and en

24 Here we sequence 30 fungal genomes, and perform transcriptomics with three r

25 FunGAP predicts protein-coding genes in a fungal genome assembly.

26 eoformans NMT allele was introduced into the fungal genome by homologous recombination.

27 Models of the evolution of fungal genomes compatible with these results, and their

28 Many plant, animal, and fungal genomes contain cytosine DNA methylation in asymm

29 Some fungal genomes contain multiple genes encoding homologue

30 ty, in a client/server relationship with the Fungal Genome Database (FGDB), and as a web-browsing too

31 and homologous TER sequences from available fungal genome databases by computational searches.

32 Many of the fungal genomes examined contain genes encoding homologue

33 SNP callers using our FDR method with three fungal genomes, finding that it was able achieve a high

34 he function of antibiotics and for exploring fungal genomes for new antibiotics.

35 To test this, we examined 100 diverse fungal genomes for the simplest type of cluster, gene pa

36 Over 40 complete fungal genomes have been publicly released with an equal

37 encoding these two proteins are found in all fungal genomes including those for the pathogens, Candid

38 rhizal lifestyle evolution, we sequenced new fungal genomes, including 13 ectomycorrhizal (ECM), orch

39 Application of the new method to known fungal genomes indicates substantial improvement over ex

40 Analysis of other fungal genomes indicates that only the budding yeasts ha

41 s that the family was represented in all but fungal genomes, indicating an ancient origin for the fam

42 A notable characteristic of fungal genomes is that genes involved in successive step

43 fy nine putative laccase-coding genes in the fungal genome of Leucocoprinus gongylophorus cultivated

44 Fungal genomes range in size from 2.3 Mb for the microsp

45 A survey of 54 fungal genomes revealed that seven other species have pr

46 The continuously expanding fungal genome sequence data have sparked genome-directed

47 t integration, analysis and dissemination of fungal genome sequences and other 'omics' data by provid

48 irst fungus in 1996, the number of available fungal genome sequences has increased by an order of mag

49 amatically based on the availability of more fungal genome sequences in recent years.

50 Of the available fungal genome sequences, only seven other closely relate

51 Although fungal genome sequencing and assembly have become trivia

52 e process of annotation in a large number of fungal genome sequencing projects.

53 (v). Different fungal genomes shared few putative orthologous PKS genes

54 Furthermore, a detailed analysis of 10 fungal genomes shows that this holozoan signature in RiB

55 ur approach to a set of nine fully sequenced fungal genomes spanning 150 million years, generating a

56 proteins amongst the 42 available sequenced fungal genomes suggests unexpected roles for circadian t

57 ated the evolution of these genes across 115 fungal genomes, testing each gene fusion for evidence of

58 coding capacity of mimivirus, the minimized fungal genomes that contain elements of bacterial metabo

59 iDB is a functional genomic resource for pan-fungal genomes that was developed in partnership with th

60 cently sequenced Drosophila genomes and nine fungal genomes to address the problem of accurate gene-t

61 We apply our procedure to seventeen fungal genomes to create a genome-wide catalogue of gene

62 -molecule long-read sequencing of 16 diverse fungal genomes, we observed that up to 2.8% of all adeni

63 splays alignments of sequences from multiple fungal genomes, while the Sequence Similarity Query tool