Sentence examples for use of comparative genomics from inspiring English sources

The current availability of well over 1000 complete bacterial and archaeal genomes permits the use of comparative genomics methods to locate the substrates for orphan TOMMs while simultaneously broadening the search for previously unknown families of post-translationally modified peptides.

The inability to predict long noncoding RNAs from genomic sequence has impeded the use of comparative genomics for studying their biology.

Two relatively new gene prediction tools that make use of comparative genomics have been deployed for analysis of the Arabidopsis Genome: Twinscan [ 20] and EuGene [ 21].

By use of comparative genomics techniques, experimental results can be transferred from one genome to another, while at the same time minimizing errors by requiring discovery in multiple genomes.

Use of comparative genomics, ecological and evolutionary facts, and the lowering costs of genomic sequencing are together aiding in the understanding of microbial diversity.

The proliferation of genome sequencing and assembly has made possible the use of comparative genomics approaches for TFBS discovery.

It is not purported to model the ancestor, even though it, same as the ancestral genomes, may be constructed using methods of comparative genomics, and even though minimal genome may be enriched in ancestral genes.

In this study, we performed a systematic genome-wide in silico screen to search for novel small ncRNAs in the genome of Trypanosoma brucei using techniques of comparative genomics.

Recently, we developed RNAcode, a gene prediction program that uses the principle of comparative genomics [ 15] to detect protein-coding genes in multiple genome alignments [ 16].

Although the type II fatty acid synthesis (FAS) pathway in Shewanella was constructed using the approach of comparative genomics (Wang et al., 2009), it seemed likely that some unusual/unclear aspects are present in the regulation of this specialized Type II FAS (Rodionov et al., 2011).

This process is best done using the possibilities of comparative genomics and multiple sequence alignments.