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Recently, the genome of T. castaneum has been sequenced to 7-fold coverage using a whole genome shotgun approach and assembled using the HGSC's assembly engine Atlas (http://www.hgsc.bcm.tmc.edu/projects/tribolium/). The present paper describes the molecular characterization of a chemoreceptor family in T. castaneum.
The genome of A. subglobosum LB-1/A1 was sequenced using a whole genome shotgun sequencing approach and assembled into 371 contigs (DDBJ BAUZ01000001-BAUZ01000371) arranged into 106 supercontigs (Table 1, Additional file 1: Figure S1).
To identify genetic factors potentially involved in CO pathogenesis in human we 1) applied comparative integratomics approach and assembled the database of all CO-associated genomic loci reported in the literature, regardless of the study approach and species, 2) presented the loci on a genomic map as human orthologs, and 3) prioritized the collected data using systems biology approach.
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Therefore, four sets of data are generated, two from MetaVir (one with unassembled and another with assembled reads) and two from our tBLASTx approach (unassembled and assembled).
Recently, the Medaka genome sequence has become accessible: the complete sequence of LG22 by BAC-based sequencing approach and the assembled sequence data from the whole-genome shotgun approach (UT genome browser).
However, to utilize comparative approaches with completely sequenced and assembled tree reference genomes as a means to identify potential candidate genes in marked intervals of less well sequence characterized species, we need to access the degree of preservation among tree genomes at a high resolution level, e.g. within 1 centiMorgan (cM) windows.
This illustrates the value of incorporating novel metagenome sequences into systematic bioprospecting efforts, and as more metagenomics data is generated and assembled, this approach is likely to become a major driver for expanding protein sequence space available for enzyme characterization.
We applied the whole-genome shotgun sequencing approach to sequence and assemble the genome of N. apis which has an estimated size of 8.5 Mbp.
The present study used a second-generation sequencing approach to determine and assemble the plastid genomes (plastomes) of four representatives from the agriculturally important Lolium-Festuca species complex of pasture grasses (Lolium multiflorum, Festuca pratensis, Festuca altissima, and Festuca ovina).
I would like to see side by side an analysis of how well the approach can identify and assemble de novo the genome of a species where the genome is known well.
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