• Nenhum resultado encontrado

Towards decrypting cryptobiosis--analyzing anhydrobiosis in the tardigrade Milnesium tardigradum using transcriptome sequencing.

N/A
N/A
Protected

Academic year: 2017

Share "Towards decrypting cryptobiosis--analyzing anhydrobiosis in the tardigrade Milnesium tardigradum using transcriptome sequencing."

Copied!
15
0
0

Texto

Loading

Imagem

Figure 1. Workflow for the de novo hybrid assembly of the M. tardigradum transcriptome
Table 1. Comparison of M. tardigradum assembly with reference genomes for the presence of 248 CEGs using CEGMA.
Figure 3. Representative results of proteome coverage analysis using est2assmbly. Reference cDNA and proteome data were from Anopheles gambiae (An.g.), Caenorhabditis elegans (C.e.), Daphnia pulex (D.p.), Drosophila melanogaster (D.m.), Ixodes scapularis (
Figure 4. BLAST annotation of transcriptome assembly.
+2

Referências

Documentos relacionados

The present investigation expands bioinformatic data available to study coral molecular physiology through the assembly and annotation of a reference transcriptome of the

Keywords Coptotermes formosanus , Transcriptome, Gene expression, Carbon dioxide response, Next generation sequencing data, Chemosensory

In this study, we describe the development of a sunflower reference transcriptome assembly based primarily on long-read ESTs, as well as the generation and analysis of

Li D, Deng Z, Qin B, Liu X, Men Z (2012) De novo assembly and characterization of bark transcriptome using Illumina sequencing and development of EST-SSR markers in rubber tree

In the pres- ent study, the Illumina RNA-seq technology was utilized to perform transcriptome analysis and SSR marker discovery in the swamp buffalo without using a reference

Six statistical tests were applied to the Forest ESTs and the number of genes with specific or preferential expression in all tests is shown in the inner and outer

In the subsection Analysis of transcriptome sequencing results of the Materials and Meth- ods section, the final sentence of the first paragraph references the incorrect

In our functional annotation, unigene sequences were first aligned using Blastx to the NR, Swiss-Prot, KEGG, and COG protein databases (E-value , 10 2 5 ), which retrieved proteins