De Novo assembly and annotation of the freshwater crayfish Astacus astacus transcriptome

被引:42
作者
Theissinger, Kathrin [1 ]
Falckenhayn, Cassandra [2 ]
Blande, Daniel [3 ]
Toljamo, Anna [3 ]
Gutekunst, Julian [2 ]
Makkonen, Jenny [3 ]
Jussila, Japo [3 ]
Lyko, Frank [2 ]
Schrimpf, Anne [1 ]
Schulz, Ralf [1 ]
Kokko, Harri [3 ]
机构
[1] Univ Koblenz Landau, Inst Environm Sci, Ft Str 7, D-76829 Landau, Germany
[2] German Canc Res Ctr, DKFZ ZMBH Alliance, Div Epigenet, Neuenheimer Feld 580, D-69120 Heidelberg, Germany
[3] Univ Eastern Finland, Dept Environm & Biol Sci, POB 1627, Kuopio 70211, Finland
关键词
Aphanomyces astaci; Genomics; RNA-seq data; Trinity; Transrate; BUSCO; PLAGUE APHANOMYCES-ASTACI; RNA-SEQ DATA; PERSISTENT INFECTION; REFERENCE GENOME; POPULATIONS; EXPRESSION; RESISTANCE;
D O I
10.1016/j.margen.2016.02.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We generated RNA-seq data to assemble the transcriptome of the noble crayfish (Astacus astacus) from four combined tissues (abdominal muscle, hepatopancreas, ovaries, green glands). A total of 194 million read pairs with a length of 100 bp were generated. The transcriptome was assembled de novo using Trinity software, producing 158,649 non-redundant transcripts. Lowly expressed transcripts were filtered out leaving 45,415 transcripts of which 14,559 were found to contain open reading frames with predicted gene function. The Transrate software revealed that 91% of the total reads were realigned to the assembly. Furthermore, BUSCO analysis indicated that our assembly is 64% complete. A total of 13,770 transcripts were assigned at least one GO term. This first de novo transcriptome assembly is an important foundation for future genomic research on the noble crayfish and adds to the general knowledge and further characterization of transcriptomes of non-model organisms. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 10
页数:4
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