The phrase "a much wider sequence" is correct and usable in written English.
It can be used when discussing a range or series that is broader or more extensive than a previously mentioned sequence.
Example: "In this study, we will analyze a much wider sequence of data to draw more comprehensive conclusions."
Alternatives: "a significantly broader range" or "a considerably larger series".
Disorder, which is encoded by a much wider portion of sequence space as compared to order, can indeed represent a strategy by which genes encoding overlapping reading frames can lessen evolutionary constraints imposed on their sequence by the overlap, allowing the encoded overlapping protein products to sample a wider sequence space without losing function.
(3) It has a strong capability to identify variants based on a relatively divergent reference genome, which brings it to a much wider application other than re-sequencing projects.
In these experiments, we recovered recombinant genomes occupying a much wider variety of positions within the sequence space than those encountered in the original study, suggesting a plausible scenario for the initial adaptation of MSV to maize.
Although the LysM domain family is relatively small compared to the top 20 PFAM domain families in terms of the number of sequences, it displays a much wider range of domain architectures than 10 of the top 20 domain families.
Based on high-throughput sequencing, we identified a much wider range of small RNAs, 18 30 nt in length (Fig. 1), with 24 nt being the most abundant, followed by 21 and then 22 nt.
Conversion rates will likely improve considerably by selecting SNPs from a sequence database built from a much wider representation of the diversity of each target species and validating in a larger panel of individuals.
On the contrary, MOD-D and MOD-E display a very high level of sequence conservation and have a much wider phyletic distribution with homologs in all fungi and higher eukaryotes.
Future studies utilizing the rapidly increasing power of genome sequencing technologies to interrogate a much wider range of candidate genes, and eventually the whole exome, for rare variants that predispose to CVM will be of great interest.
As our aim is to include as many independent domestic lineages as possible, there is a much wider availability of mitochondrial genomes than whole nuclear genome sequences.
However, more comprehensive studies on a much wider range of eukaryotic taxa are now feasible as many sequences of complete or nearly complete genomes together with their transcripts have become available.
