DNA Sequencing
Species
Analyte
Platform
Brand
Industry
Results 11
NGS Bovine SkimSEEK™
SKU No. 901
Low-pass skim sequencing & imputation from Neogen® Genomics
Species: Bovine
NGS Bovine 10x WGS
SKU No. 904
Sequencing provides the potential to more accurately access the genetic potential of organisms earlier in life while providing an in-depth look into the bioinformatics that explore the full genome.
Species: Bovine
NGS Bovine 30x WGS
SKU No. 905
Sequencing provides the potential to more accurately access the genetic potential of organisms earlier in life while providing an in-depth look into the bioinformatics that explore the full genome.
Species: Bovine
Tilapia SkimSEEK™
SKU No. 190139
Low-pass skim sequencing and imputation for Nile tilapia from Neogen® Genomics and the Center for Aquaculture Technologies (CAT).
InfiniSEEK™
SKU No. 190069
A high-throughput sequencing technology that provides deep and wide genomic information allows access to cutting-edge genomic information.
Species: Bovine
$55.00 each
MiSeq Reagent Kit v3 (150-cycle)
SKU No. 11504
The Illumina MiSeq v3 150-cycle kit generates 20–25 million read-pairs with an approximate output of 3.3–3.8 Gb.
MiSeq Reagent Kit v2 (300-cycles)
SKU No. 11500
The Illumina MiSeq v2 300-cycle kit generates 12–15 million read-pairs with an approximate output of 4.5–5.1 Gb.
MiSeq Reagent Kit v2 (500-cycles)
SKU No. 11501
The Illumina MiSeq v2 500-cycle kit generates 12–15 million read-pairs with an approximate output of 7.5–8.5 Gb.
MiSeq Reagent Kit v3 (600-cycle)
SKU No. 11502
The Illumina MiSeq v3 600-cycle kit generates 20–25 million read-pairs with an approximate output of 13.2–15 Gb.
NovaSeq 6000 S4 Prepared Pool v1.5 (200 cycles)
SKU No. 11505
The Illumina NovaSeq 6000 200-cycles prepared pool generates 16–20 billion paired-end reads (8–10 billion single-end reads), with an approximate output of 1600–2000 Gb.
NovaSeq 6000 S4 Prepared Pool v1.5 (300 cycles)
SKU No. 11503
The Illumina NovaSeq 6000 300-cycles prepared pool generates 16–20 billion paired-end reads (8–10 billion single-end reads), with an approximate output of 2400–3000 Gb.
The future of genomic innovation is here with DNA sequencing technology. Equipped with the latest and most powerful whole genome sequencing technologies, we can supply the most comprehensive genomic solutions and analysis available in the market.
The technology allows you to capture genetic variants from a single sample to accelerate discovery and genomic progress for all species. We’re leveraging the next generation of sequencing technologies and our industry expertise to provide comprehensive whole genome solutions with an emphasis on quality and quick turnaround time.