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Our results confirm that, for at least one of the technologies, repeats are effectively the sole cause of assembly gaps, but only when excessive coverage is used.
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Both examples reveal the complexity inherent to the de Bruijn graph even on a small set of reads and provide insight into possible causes of assembly errors.
Finally, they provide large similarity segments that are rich in repetitive sequences, which are the cause of frequent assembly errors.
By comparison to the E. tenella plastid genome [ 23] we inferred the repeat structure of the ribosomal genes (two inverted repeats) as the likely cause of the assembly problems.
The cause of self-assembly has been studied through spectroscopic techniques like FTIR and UV vis measurements revealing strong interaction between polymer chain (both hard and soft segments) and graphene which is further confirmed from the depression of melting point and decrease in heat of fusion with increasing graphene content in the nanohybrids.
Because these 950-bp repeats are longer than any individual reads, they are not spanned by any single sequence; such repeats are a common cause of mis-assemblies.
Activation of Rho protein causes to assembly of the actin-myosin contractile filaments into focal adhesion complexes that leads to cell polarity and facilitate motility [ 7].
In order to identify possible causes of incomplete assembly, the noncoding intergenic spacers were analyzed for secondary structure formation.
If the number of hydrogen bonds were the root cause of the different assembly behavior, then one would expect A and T to assemble similarly to each other.
Heinrich points out strategic advantages of an indirectly elected UNPA: "Another advantage to basing representation in a UN Parliamentary Assembly on national parliaments is that it may engage parliamentarians as allies in the cause of getting the assembly established, and, later, helping to build the political will for its evolution.
We conclude that the primary cause of the separate assembly of homoeologous contigs is the divergence of the intergenic spaces of homoeologous chromosomes.
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