Sentence examples for using a deep sequencing from inspiring English sources
Using a deep sequencing approach, we analyzed TCRβ repertoires longitudinally over approximately 20 years, with ages ranging from 23 to 50 years at the start (23 to 65 years overall), in peripheral-blood CD4 and CD8 T-cell populations that were collected and cryopreserved 3 times at intervals of approximately 10 years from each of 6 healthy adults (3 men and 3 women).
The aim of this study was to characterise the miRNA regulation layer taking place in porcine DCs in the course of PRV infection using a deep sequencing approach.
Using a deep sequencing strategy, a number of miRNAs expressed during three anther development stages of cotton were identified.
Additional mutations were found with this procedure and the results obtained by ddPCR were validated using a deep sequencing method.
Using a deep sequencing approach, a large group of evolutionarily young miRNA genes was discovered in Drosophila [ 9].
This comprehensive screen for E. coli sRNAs using a deep sequencing approach has shown that many as-yet-undiscovered sRNAs are potentially encoded in the E. coli genome.
Given that miRNAs contribute significantly to the pathophysiology of breast cancer by contributing to invasion and metastasis [20], [21], [22], [23], epithelial to mesenchymal transition [24], [25], and maintenance of breast stem cells [26], we have used a deep sequencing approach to identify novel miRNAs in human breast cancer cell lines that exhibit diverse tumorigenic potential.
In this study, we used a deep sequencing approach to investigate the fungal community structure in the tubers of G. flavilabella and in the surrounding soil.
We used a deep sequencing platform to extensively profile and identify changes in the miRNAs expression that occurred under sulfur-replete and sulfur-deprived conditions.
To investigate the role of Chlamydomonas reinhardtii miRNAs involved in sulfur deprivation, we used a deep sequencing platform to extensively profile and identify changes in the miRNAs expression that occur during sulfur-replete and sulfur-deprived conditions.
In order to isolate and analyze the miRNAome of artichoke, we used a deep sequencing approach on four sRNA libraries obtained from two tissues, leaves and roots, in standard conditions and under saline treatment.
