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=== SINGULAR GENOMICS ===
=== SINGULAR GENOMICS ===
The [[BioMicroCenter|BioMicro Center]] provides support for sequencing on the Singular G4. This short read sequencer uses the similar sequencing-by-synthesis chemistry as Illumina with modest modifications and a patterned flowcell. Critically, the G4 allows addressable lanes at very competitive [[BioMicroCenter:Pricing|pricing]].
The [[BioMicroCenter|BioMicro Center]] provides support for sequencing on the Singular G4. This short read sequencer uses four color sequencing-by-synthesis chemistry on a patterned flowcell. Critically, the G4 allows addressable lanes at very competitive [[BioMicroCenter:Pricing|pricing]].


=== ELEMENT BIOSCIENCES ===
=== ELEMENT BIOSCIENCES ===

Revision as of 18:00, 9 June 2025



HOME -- SEQUENCING -- LIBRARY PREP -- HIGH-THROUGHPUT -- COMPUTING -- OTHER TECHNOLOGY

SHORT READ SEQUENCING

ILLUMINA

The BioMicro Center provides broad support for Illumina sequencing. The Center has one MiSeq and access to various NovaSeq Xplus units. We support a wide variety of applications, such as ChIP-Seq, miRNA sequencing and RNA-seq. Each lane can potentially accommodate dozens of indexed samples (depending on sequence complexity and desired coverage). Read lengths vary, depending on users, between 20nt and 325nt per end.

Illumina Sequencing is performed on a lane-by-lane basis for a specific number of reads or entire flowcells. This enables us to support a very broad spectrum of Illumina Library types as well as handle custom sequencing applications.

SINGULAR GENOMICS

The BioMicro Center provides support for sequencing on the Singular G4. This short read sequencer uses four color sequencing-by-synthesis chemistry on a patterned flowcell. Critically, the G4 allows addressable lanes at very competitive pricing.

ELEMENT BIOSCIENCES

The BioMicro Center provides support for the Element AVITI24, which utilizes both standard avidity sequencing on a random flowcell and direct in situ sequencing with Teton Cytoprofiling.

LONG READ SEQUENCING / PACBIO and OXFORD NANOPORE

The BioMicro Center has made significant investments in long read sequencers. The Center has access to two separate platforms: Pacific Biosciences Sequel and Oxford Nanopore PromethION P2 Solo.

Pacific BioSciences sequencing is no longer available at the BioMicro Center. The Center is able to provide outsourcing to sister facilities to enable access to the REVIO.

Oxford Nanopore Sequencing is still a new technology in the core but we are developing expertise that may be useful to researchers on campus. The center houses two Oxford Nanopore PromethION P2 Solos. Contaminants known to cause issues on the Nanopores so far include: EDTA, ethanol, isopropanol, NaCl, guanidinium chloride, guanidinium isothiocyanate, and phenol. Nanopore requests can be made through iLabs.

Beyond the sequencers, the BioMicro Center has additional tools that are critical to long read sequencing. These include an AATI FemtoPulse and a Sage BluePippin.

SANGER SEQUENCING

The MIT BioMicro Center *does not* support Sanger sequencing. Many third party providers exist for this method. For those who prefer to utilize core facilities instead of commercial providers, Sanger sequencing is available through the DF/HCC DNA Resource at the Dana-Farber Cancer Institute