Sentence examples for discovery of nucleotide from inspiring English sources

The discovery of nucleotide diversity captured as single feature polymorphism (SFP) by using the expression array is a high-throughput and effective method in detecting genome-wide polymorphism.

With the recent discovery of nucleotide changes associated with LP comes the prospect of direct genetic tests for the trait [ 8- 10].

Subsequently, high throughput discovery of nucleotide variation was performed using sequences with more than 90% reliability by using the assembled contigs that were 50 bp or longer as the reference sequence.

This is compatible with the discovery of great nucleotide variation in ITS region among isolates of P. noxius found in Taiwan in this study.

The genome-wide discovery of single nucleotide polymorphisms (SNPs), even among closely related cultivars, has enhanced the power of allele mining in a wide range of rice breeding materials.

Current methods focus on the discovery of single nucleotide polymorphisms (SNPs) associated with disease traits.

Exome-targeted resequencing analysis is particularly useful for the discovery of single nucleotide variants (SNVs) and insertion or deletions (indels).

Transcriptome sequencing enables efficient high-throughput discovery of single nucleotide polymorphism (SNP) markers for a complex polyploid species.

This combined assembly (Additional file 2), was used as the reference sequence for the discovery of single nucleotide variants (SNVs).

Several high-impact studies have provided draft genome sequences of many strains of the same species [ 22 25], where genome alignments allow the discovery of single nucleotide differences.

Therefore, we evaluated the impact of different software tools and analytical approaches on the discovery of single nucleotide polymorphisms (SNPs) in multiplexed tNGS data.