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Rutgers - New Jersey Medical School

MiSeq

Access focused applications such as targeted resequencing, metagenomics, small genome sequencing, targeted gene expression profiling, and more. MiSeq reagents enable up to 15 Gb of output with 25 million sequencing reads and 2 × 300 bp read lengths.
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Rutgers - New Jersey Medical School

MiSeq

$946.00$2,376.00
Access focused applications such as targeted resequencing, metagenomics, small genome sequencing, targeted gene expression profiling, and more. MiSeq reagents enable up to 15 Gb of output with 25 million sequencing reads and 2 × 300 bp read lengths.
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Base Pair Biotechnologies, Inc.

iSeq 100

$1,200.00
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Admera Health, LLC

NovaSeq 6000

$5,500.00$18,200.00
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Admera Health, LLC

Sequel II

$3,000.00
The Sequel II System has been recognized for its ability to generate longer reads with greater accuracy and throughput, at a significantly lower cost.
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Admera Health, LLC

Sequel

$2,200.00$3,000.00
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Admera Health, LLC

NextSeq 550

$1,580.00$6,648.00
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Admera Health, LLC

HiSeq X

$1,430.00
HiSeq X Ten System delivers > 18,000 human genomes per year; HiSeq X Five System delivers > 9000 human genomes per year. Take advantage of industry-leading data quality with the highly accurate Illumina sequencing by synthesis technology. Now enabling cost-effective whole-genome sequencing of nonhuman species with unrivaled throughput.
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Admera Health, LLC

MiSeq

$419.00$2,198.00
Access focused applications such as targeted resequencing, metagenomics, small genome sequencing, targeted gene expression profiling, and more. MiSeq reagents enable up to 15 Gb of output with 25 million sequencing reads and 2 × 300 bp read lengths.
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Tormod Inc.

MiSeq

$199.89$299.89
Access focused applications such as targeted resequencing, metagenomics, small genome sequencing, targeted gene expression profiling, and more. MiSeq reagents enable up to 15 Gb of output with 25 million sequencing reads and 2 × 300 bp read lengths.
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State University of New York at Buffalo

NovaSeq 6000

$4,089.40$51,860.03
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Strand Analytics Whole Exome

$150.00
Variations are identified using Strand's integrated proprietary software STRAND®NGS - which provides analysis, management and visualization tools for next-generation sequencing data, and interpreted using Strand's proprietary interpretation and reporting platform StrandOmics™ -   which combines bioinformatics algorithms, public data from external sources/knowledge databases, visualization interfaces and reporting capabilities.
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