Not exact matches
Nextera
library construction and Illumina
sequencing provided the most complete genome assembly and reliable intrahost single - nucleotide variant (iSNV, frequency > 0.5 %) identification (6).
High - throughput automated barcoding and
library construction for powerful new
sequencing applications.
Construction of
libraries and
sequencing with the Illumina HiSeq 2500 platform were performed by Berry Genomics.
Three micrograms of total RNA was used for the polyA +
library construction using a TruSeq SBS
Sequencing Kit, version 3.
Although the
construction and
sequencing of an individual SAGE
library is expensive and laborious compared to microarray analysis, SAGE offers the invaluable potential for gene discovery as the analysis is not limited to genes represented on an array.