Sentence examples for discovery sequence from inspiring English sources

Here we present the first comprehensive review and analysis of EFE, including its discovery, sequence diversity, reaction mechanism, predicted involvement in diverse metabolic modes, heterologous expression, and requirements for harvesting of bioethylene.

These 34 regions cover 1.84 Mb or 0.07% of the autosomal genome, and many of the CNV positions coincided between the two reports [ 16] and [ 17] even though the authors have used different type of data as source of information for CNV discovery, sequence and SNPs, respectively.

For low-pass SNP discovery sequencing, 10X-15X coverage will allow genotyping of a minimum of 65% of the parasite genome using either the standard library preparation method or the whole genome capture protocol.

The Cancer Genome Atlas (TCGA) [ 8], a consortium focused on research and discovery, sequenced the entire exome of tumors but at limited coverage depth, rejecting specimens with less than 60% cellularity and preventing the reliable identification of subclonal mutations.

The GS-FLX has been already employed in bacterial genome sequencing, miRNA discovery, cDNA sequencing, ultra-deep sequencing of PCR amplicons and in other fields of application.

The development of powerful new methods for DNA sequencing enable the discovery of sequence variants, their utilization for the mapping of mutant loci, and the identification of causal variants in a single step.

Recent developments in sequencing technology have simplified and accelerated the discovery of sequence variants, enabling development of sequence-based markers including single nucleotide polymorphisms (SNPs) and insertion/deletion polymorphisms (InDels) [ 21].

Recent developments in sequencing technology have simplified and accelerated the discovery of sequence variants, enabling the development of sequence-based markers including single nucleotide polymorphisms (SNPs) and insertion/deletion polymorphism (InDel) markers [ 14].

Then we step through elements of the workflow in greater detail, including a brief overview of the discovery of sequence variations from high-throughput sequence data.

Large-scale sequencing projects offer a possibility for low cost SNP discovery since sequence variants can be found computationally by analysing the redundancy in sequence databases.

Next generation sequencing approaches are considered highly reliable for genome-wide discovery of sequence variation [ 15], when used to compare different lines/strains to a reference genome [ 58].