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Capabilities // Our Newest Instruments

Illumina NextSeq 1000

Get the Illumina confidence you know and love with the benchtop NextSeq 1000 instrument.

Advanced XLEAP-SBS chemistry enables faster, more economical, and higher quality sequencing than ever before. Perfect for sequencing projects that require a quick turnaround. 

What Can You Do?
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Whole Exome Sequencing

Sequence protein-coding genomic regions on a shorter timeline than other sequencers. These regions make up less than 2% of the human genome, but they contain about 85% of known disease-related variants.

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Single-Cell Sequencing

Understand heterogeneous sample types, changes at different points in the cellular life cycle, and individual cells' response to stimuli or therapeutics. 

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Amplicon Sequencing

Perform deep sequencing of PCR products (amplicons) to detect and analyze genetic variants including low-abundance variants, SNPs, and clone verification. 

 

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Transcriptomics

Run bulk RNA sequencing projects for a broad view of the transcriptome. Simultaneously detect known and novel elements, including alternative transcript isoforms, gene fusions, and other features.

NextSeq 1000 Specifications

Available Flow Cells

  • P1
  • P2

Output Range

10–240 Gb

Single-End Reads per Run

100M–400M

Maximum Read Length

2 x 300 bp

Available Data Analysis

Genomic analysis: 

  1. Single Nucleotide Variants (SNV)
  2. Insertions and Deletions (Indel)
  3. Copy Number Variants (CNV)
  4. Structural Variants (SV)
  5. Somatic Mutation Identification
  6. Annotated Reporting
  7. Family Trio Analysis
  8. Pathogenicity Scoring
  9. Phenotype Relationship

Transcriptomic analysis:

  1. Gene Expression
  2. Alternative Splicing
  3. Novel Transcript Identification
  4. Isoform Identification
  5. Variant Annotation
  6. Single Nucleotide Variants (SNV)
  7. Fusion Gene Identification
  8. Novel Alternative Transcript Identification
  9. Differential Gene Expression (DEG)
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