DNA Sequencing Products & Reviews

Fastest, most efficient methylated DNA enrichment method on the market

Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants

Transcriptome profiling by RNA-Seq

Insights into the diversity of microbial communities

Reliable detection of cancer-associated mutations in 597 genes from liquid biopsy samples

For low-to-medium throughput NGS needs, the Zephyr™ G3 NGS workstation is a compact, semi-automated solution designed to construct up to 96 NGS libraries per day. This compact workstation is equipped with a highly precise, 96-channel pipetting head and includes an integrated gripper. For Research Use Only. Not for use in diagnostic procedures.

High-throughput, low-volume automated platform for NGS library preparation.

Comprehensive profile of all mutations present in the exome

SMARTer Apollo NGS library prep system

Bionano Data Solutions™ includes a complete suite of hardware and software for end-to-end experiment management, analysis and bioinformatics processing, along with convenient web-based management and monitoring tools.

The MiSeq FGx is the first fully-validated next generation sequencing (NGS) solution designed specifically for the challenges of human genetic identification.

Automated, preparative gel electrophoresis systems, used for accurate and reproducible size selection/collection of DNA (or cDNA) fragments, for the preparation of libraries for next generation sequencing (NGS)

Don’t risk wasting your precious sequencing samples. Diagenode’s validated iDeal ChIP-seq kit for Histones has everything you need for a successful start-to-finish ChIP of histones prior to Next-Generation Sequencing. The complete kit contains all buffers and reagents for cell lysis, chromatin shearing, immunoprecipitation and DNA purification. In addition, unlike competing solutions, the kit contains positive and ne…

Tagmentation is a reaction where an enzyme (a transposase) cleaves DNA and incorporates sequencing adaptors at the ends of the DNA fragments in one step. In our ChIPmentation technology we combine chromatin immunoprecipitation and tagmentation in one streamlined workflow where the tagmentation step occurs directly on chromatin. The TAG Kit for ChIPmentation has been developed for researchers who would like to perform Ch…

The complete synthetic reference material D614G is a full-length synthetic genome encoding the D614G spike protein mutation with a T7 promoter and a poly(A) tail. Genome modifications and editing are available.

Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.

Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.

Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.

Kit for the enzymatic fragmentation of dsDNA

Plasma-SeqSensei™ (PSS) CRC RUO Kit allows the highly sensitive and specific detection of mutations in circulating tumour DNA (ctDNA) from plasma of patients with colorectal cancer (CRC).

The Plasma-SeqSensei™ (PSS) Melanoma RUO (research use only) Kit allows the highly sensitive and specific detection of mutations in circulating tumour DNA (ctDNA) from plasma of patients with melanoma cancer.

The Plasma-SeqSensei™ (PSS) NSCLC RUO (research use only) Kit detects mutations in circulating tumour DNA (ctDNA) from plasma in patients with non-small cell lung cancer.

The Plasma-SeqSensei™ (PSS) Thyroid Cancer RUO (research use only) Kit detects mutations in circulating tumour DNA (ctDNA) from plasma in patients with thyroid cancer.

Next-generation sequencing research services for SARS-CoV-2 variant surveillance.

Looking for consistent and reproducible single cell results across experiments, across users, and even across multiple sites? With Chromium Connect, you can combine single cell partitioning, barcoding, and library preparation in a standardized, automated workflow.