library preparation

Admera Health is a genomics and multi-omics service provider based in South Plainfield, New Jersey, offering RNA-seq, single-cell RNA-seq, spatial transcriptomics, whole genome sequencing, and bioinformatics services to academia, biotech, and biopharma. Its CLIA-certified, CAP-accredited laboratory operates entirely in the US and is a certified service provider for 10x Genomics, PacBio, Parse Biosciences, IDT, and Takara Bio's Shasta system.

bioinformatics analysislong-read sequencingmulti-omics integrationnucleic acid extractionRNA-seqsingle-cell RNA-Seqspatial transcriptomicswhole genome sequencing

AmpSeq is a next-generation sequencing (NGS) company by scientists for scientists with over 15 years of experience. It provides end-to-end sequencing services from project design to bioinformatics analysis, including sample extraction, library preparation, sequencing, and data analysis, with industry-leading turnaround times. Labs are located in Boston, Maryland, and Connecticut.

bioinformatics analysisdata analysisHi-C sequencingprimer designRNA sequencingsample extractionsequencingtargeted sequencingwhole genome sequencing

BreakSight® Inc. spun out of research in Dr. Eric Brown's laboratory at the University of Pennsylvania, where Nishita Shastri developed the BrITL technique to tag and retrieve DNA double-strand break ends from the genome. The company provides commercial assays and services for genome-wide DNA break mapping, bioinformatics analysis, and precision medicine research, aiming to expand coverage to the non-coding 98% of the genome.

bioinformatics analysisDNA double-strand break mappingnext-generation sequencingpeak callingquality controlRNA-seq analysis

Complete Genomics Incorporated operates an online store offering genomic sequencing reagents, library prep kits, extraction kits, lab automation consumables, and sequencing flow cells for DNBSEQ sequencing platforms. The company is located at 2904 Orchard Parkway, San Jose, California. Products are marked for research use only, not for diagnostic procedures.

automated extraction platformsexome capturehigh-throughput sequencingnucleic acid extraction

Daicel Arbor Biosciences provides tools and services for genomics and protein engineering research, including next-generation sequencing, cytogenetics, and cell-free protein expression. The company manufactures its products in-house and offers customized solutions tailored to research needs.

Bioinformaticscell-free protein expressionDNA & RNA extractionhybridization capturein-house manufacturingin situ hybridization probe designlong-read sequencingoligo pool synthesis

Divergene is a technology company providing AI-driven analytics and informatics for cell & gene therapy and bioprocessing. It offers a bioinformatics platform and AI framework for next-generation sequencing analysis, vector engineering, and vector quality control, and provides AI-driven digital-twin simulation of bioreactors and bioprocesses. The team includes Ph.D.-level bioinformaticians, data scientists, and AI experts.

AI-driven digital-twin simulationBioinformaticsbioprocess modelingcapsid engineeringnext-generation sequencingQCsequencing analysisvector engineeringvector quality control

Element Biosciences develops and manufactures benchtop sequencing and multiomics platforms, including VITARI, AVITI24, AVITI, and AVITI LT. Its systems are built on Avidite Base Chemistry (ABC) and support sequencing, cell screening, and spatial profiling. The company states its mission is to empower the scientific community with more freedom and flexibility to accelerate impact on humanity.

Avidite Base ChemistryCRISPR screeningDNA sequencingdrug screeninggenotyping-by-sequencingRNA sequencingrolling circle amplificationsingle-cell multiomicsspatial profilingtargeted sequencing

Eremid Genomic Services provides customized contract research services for research and CLIA-certified, CAP-accredited genomics applications for AgBiotech, Food & Nutrition, and Human Health organizations, combining genomics and bioinformatics services. It is a PacBio certified service provider and describes itself as one of the most capable genomics laboratories in North America.

10x Genomicsbioinformatics analysischromatin accessibility analysisCLIA-certified, CAP-accredited testinggenome assembly and annotationIllumina sequencingmethylation profilingmicrobiome analysisNanoStringOxford Nanopore TechnologiesPacBio SMRT sequencingRNA and DNA extractiontargeted sequencingwhole exome sequencingwhole genome sequencing

Genohub is a one-stop shop and marketplace for next-generation sequencing (NGS) and bioinformatics services, connecting researchers and clinicians with a curated network of over 100 partnering service providers. Genohub offers free scientific consultation, quality and turnaround time guarantees, and secure online project management tools for tracking projects, accepting quotes, and sharing files.

bioinformatics data analysisdata transfer and storagenext-generation sequencingoptical genome mappingOxford Nanopore sequencingproject management

Illumina applies innovative sequencing and array technologies to the analysis of genetic variation and function, serving life science research, translational and consumer genomics, and molecular diagnostics. The company describes its mission as improving human health by unlocking the power of the genome, offering next-generation sequencing and microarray solutions from benchtop to production scale, along with bioinformatics software and support.

bioinformatics and data analysisin vitro diagnostic testingmethylation profilingmicroarray genotypingnext-generation sequencingsingle-cell RNA-Seq