Sentence examples for multiple similar sequences from inspiring English sources

Instead of assigning the maximum similarity among all sequences associated with a particular term v, GOtcha aggregates the evidence collected from multiple similar sequences (Martin et al., 2004).

Indeed, the presence of multiple similar sequences in a dataset, due for example to allelic or splice variants, would lead to an overestimation of the number of genes if not corrected for internal redundancy.

Since the database is designed to find sequences that are 98% identical by BLAST, multiple highly similar sequences do not need to be retained.

When using a larger set of reference mutations, and with multiple highly similar sequences, the problem of finding a relaxed value for read percentage with non-reference nucleotide that allowed detection of the entire mutation set was amplified.

This approach does not discriminate between separate introgressions of multiple compositionally very similar sequences from a common donor, and the post-acquisition intragenomic dispersal of a large Genomic Island.

A key computational challenge in RNA-seq data analysis is to discern reads among multiple potential sources with similar sequences.

Multiple sections of highly similar sequences may well explain some of the difficulties that were encountered with sequence alignment of the MHC reference.

The cooperative binding of multiple RBDs that recognize similar sequences allows realizing a wide range of binding specificities and affinities to different mRNAs.

Given the high genetic diversity of dpo and their variable truncation patterns, a classical phylogenetic approach requiring multiple alignment of highly similar sequences, is not suitable to analyze their overall evolutionary relationships, especially for recombinant ones (Bapteste et al. 2012).

The focus in this study is on the recently active IS elements (raIS), which are defined as IS elements with multiple copies of highly similar sequences in the same genome [ 34].

One strategy that has been used to develop accurate allele calls for MPS-based STR data was the development of reference sequences for known alleles for each STR marker, and subsequent mapping of the MPS data against the set of references for each marker using stringent sequence similarity requirements (to ensure assembly to the correct reference sequence among multiple similar references) [87].