Molecular Biology Core Facilities
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Instrumentation


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Genomics Core Instrumentation
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(1) Illumina NovaSeq X Plus Sequencing platform
(1) 
Illumina NovaSeq 6000 Sequencing platform
(5) Illumina NextSeq 500  Sequencing platform
(3) Illumina MiSeq Sequencing platform
(1) Illumina MiniSeq Sequencing platform
(2) Beckman Coulter Biomek i7 robotic workstation
(1) Formulatrix Mantis liquid handler
(2) Sage Pippin Prep
(2) ABI 7900HT RT-PCR Real-Time PCR system
(1) Roche LightCycler 480 qRT-PCR system
(4) ABI 9700 Thermocycler
(4) ABI 9800 Thermocycler
(3) Bio-Rad C1000 Touch thermal cycler
(2) Agilent TapeStation 2200
(1) Agilent Bioanalyzer 4200
(1) Agilent Fragment Analyzer 5200
(2) Life Tech Qubit Fluorometer
(1) BioTek Synergy LX Plate Reader

ILLUMINA SEQUENCING PLATFORMS


High Output (800M - 25B reads)

Illumina NovaSeq X Plus
The latest addition to our Illumina sequencing fleet. NovaSeq X is an advanced version of the NovaSeq series, featuring improved technologies for even higher throughput and increased efficiency providing data faster and more affordably than ever before.

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​Illumina NovaSeq 6000

The NovaSeq 6000 is a high-throughput sequencer capable of handling large-scale genomic projects. It is known for its exceptional speed and scalability, making it suitable for applications such as whole-genome sequencing, exome sequencing, and population-scale genomics.

Mid Output (120-400M reads)

Illumina NextSeq 550
The NextSeq 550 is a mid-throughput sequencer that provides high-quality sequencing data with a faster turnaround time. It is versatile, supporting a wide range of applications, including whole-genome sequencing, targeted sequencing, and transcriptome analysis.

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Low Output (1-30M reads)

Illumina MiniSeq
The MiniSeq is a compact benchtop sequencer designed for small to medium-scale sequencing projects. It offers flexibility and efficiency, making it suitable for targeted sequencing and small whole-genome projects.
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Illumina MiSeq
The MiSeq is a benchtop sequencer designed for smaller-scale sequencing projects. It is commonly used for targeted sequencing, amplicon sequencing, and small genome sequencing.
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Contact US: [email protected]
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©2024 Molecular Biology Core Facilities at Dana-Farber Cancer Institute
  • HOME
  • ABOUT US
  • SERVICES
    • Sequencing Only
    • RNA Services >
      • mRNAseq
      • TotalRNAseq
      • Low Input mRNAseq
      • Low Input TotalRNAseq
      • Targeted RNAseq
      • small RNAseq
    • DNA Services >
      • Whole Genome Sequencing
      • Whole Exome Sequencing
      • Methylation Profiling
      • ChIPseq/Cut & Run
      • ATACseq
    • Single Cell Sequencing Services
    • Bioinformatics Services >
      • RNAseq (VIPER)
      • Peak Calling
      • Copy Number Analysis
      • Variant Calling
    • Instrumentation
  • SAMPLE SUBMISSION
  • DATA TRANSFER
  • PRICING
  • FAQ