This is achieved by accelerating the sequences of formations of plastic hinges by the implementation of reduced beam sections in a calculated manner and then compensating for the loss of the global carrying capacity of the structure.
In this research, we developed a novel fast homology search method that uses hash tables, and then applied our subsequence clustering technique to the index to further accelerate the sequence homology search algorithm.
Recently, the development of next-generation sequencing technology has dramatically accelerated the sequencing of the genomes of diverse organisms.
The main idea is to use numerical methods designed for accelerating the convergence of numerical sequences.
STEME [ 86] is a speed up of MEME in which sequences are indexed with a suffix tree for accelerating the EM steps in which sequences have to be scanned with the profile currently being optimized, and feasible time requirements also for ChIP-Seq data are reported.
Our method for accelerating the convergence of DeTemple type sequences is more general than the method introduced in [11] and [15] by Mortici.
High throughput sequencing is accelerating the rate of discovery of disease-linked loci, yet many of these uncovered genes have no known function.
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].
Connecting animal phenotypes associated with the QTL anchored on genomic sequence level with putative underlying genes would accelerate the identification of sequence polymorphisms and gene variants and the development of SNP markers for validation of association substantially.
The second aim was to accelerate the detection of sequence and copy number variations (CNV) in the selected candidate genes with lower costs, especially for the genes that are potentially involved in MR. Six DNA samples were used in this study, including two controls containing known pathogenic variants.
