NGS-Sequencer (NextSeq500)

Illumina NextSeq500. Sequencing Rates per run. All pricing includes kits and total number of sequencing hours required per run. This instrument is used after DNA or RNA have been converted to NGS libraries at the core. This instrument is used for sequencing DNA or RNA libraries to detect genomic variants in any organism. It can be used to detect single nucleotide polymorphisms (SNPs), insertions and deletions (INDELS), gene duplication events, and chromosomal rearrangements. Additionally, sequencing total RNA, small RNA, or mRNA can reveal information about gene expression levels, presence/absence of gene expression, gene splice variants, gene fusion events, and SNPs.