bioinformatics analysis

AccuraScience is a bioinformatics and computational biology service company founded in June 2013, described as the first bioinformatics service company in the U.S. to offer broad-spectrum, fully customized analysis for academic and industry researchers. It has completed more than 400 projects for over 180 institutions worldwide, and its team brings over 200 years of combined experience in bioinformatics, computational biology, and the life sciences.

16S and shotgun metagenomicsAlphaFold structural modelingATAC-seq/ChIP-seq/CUT&Tag/CUT&RUN analysiscomputational biologyDNA methylation analysisGWAS/EWAS/TWAS/PWASHi-C and 3D genome analysisLC-MS, GC-MS, NMR data analysismachine learning and deep learning modelingmulti-omics integrationNIH NAM grant support and modelingproteomics pipelines (DIA/TMT)RNA-seq analysissingle-cell and spatial transcriptomicsvariant callingwhole-genome/exome analysis

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.

library preparationlong-read sequencingmulti-omics integrationnucleic acid extractionRNA-seqsingle-cell RNA-Seqspatial transcriptomicswhole genome sequencing

Alacris Theranostics GmbH is a systems medicine company based in Berlin offering next-generation sequencing (NGS) and bioinformatics services for research, pharma, and precision medicine. It provides end-to-end NGS workflows from sample collection to data analysis, and operates an ISO 15189 medically accredited laboratory. Its Alacris-CMTA® platform delivers Deep Comprehensive Genomic Profiling for personalized cancer diagnostics.

clinical NGS analysisgenomic and epigenomic analysisISO 15189 accredited laboratorymetagenomicsnext-generation sequencingRNA-seqsingle-cell sequencingspatial transcriptomicstranscriptomic analysiswhole exome sequencingwhole genome bisulfite sequencingwhole 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.

data analysisHi-C sequencinglibrary preparationprimer designRNA sequencingsample extractionsequencingtargeted sequencingwhole genome sequencing

Arraystar Inc provides innovative tools and sample-to-data services for non-coding RNA research, offering comprehensive and systematic analysis for expression profiling and regulation of RNAs, especially regulatory non-coding RNAs (ncRNAs). The company uses cutting-edge science and state-of-the-art technologies to empower biomedical science researchers.

CUT&TagLC-MS mass spectrometrylibrary constructionmicroarray analysisreal-time QPCRRNA blottingRNA modification sequencingRNA sequencing

BioData Sage LLC is a Women-owned small business with over 10 years of experience working in Government across multiple institutes and centers across the National Institutes of Health. It guides clients across industry, academia, government, and the non-profit sector in harnessing the power of data, offering tailored strategic planning, consulting, training, and community engagement services.

cloud platform integrationcommunity engagementdata management reviewhackathon organizationstatistical modelingstrategic planning for data sciencetraining program development

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.

DNA double-strand break mappinglibrary preparationnext-generation sequencingpeak callingquality controlRNA-seq analysis

Bridge Informatics provides professional bioinformatics services for biotech and pharma, helping life science companies translate genomic data into biological results. Its team of biologists, computational scientists, software engineers, and bioinformaticians offers bioinformatics analysis, data management, data mining, cloud architecture and maintenance, software and database engineering, publication services, and flexible staffing solutions. It also offers Bridge Horizon, a cloud platform for running pipelines at scale and managing data.

cloud architectureCloud maintenancecomputational biologydata miningdata visualizationPipeline developmentpublication servicesSoftware & database engineeringstaffing solutions

Cellecta, Inc. is a genomics company based in Mountain View, CA that provides products and services for drug target and biomarker discovery, including CRISPR and RNAi screening libraries, lentiviral constructs, cell barcoding libraries, and transcriptome and adaptive immune receptor profiling kits. The company offers both do-it-yourself and full-service options for targeted and genome-wide screens.

adaptive immune receptor profilingcell line engineeringCRISPR/RNAi screeningcustom library constructionlentiviral vector packagingmultiplex PCRNGSsingle-cell genetic analysistargeted RNA-Seq expression profiling

ClickSeq Technologies LLC provides Next-Generation Sequencing services and kits based on its patented ClickSeq™ library preparation method, which uses Click-Chemistry in place of fragmentases and ligases. Offerings include RNAseq, DNAseq, Poly(A)-targeted and template-targeting sequencing, sequencing on Illumina platforms, and bioinformatics support and analysis.

custom primer designlibrary synthesisnext-generation sequencingsequencing on Illumina platforms

Data2Bio is a contract research organization founded in 2010 that provides genomics, genotyping, and genomic selection services. It offers SNP discovery, RNA-seq, high-throughput genotyping, gene mapping, and breeding support to clients on six continents working on over 30 species, from major crops and livestock to orphan and nascent crops. Its proprietary tGBS genotyping-by-sequencing technology enables accurate genotyping of heterozygous individuals and polyploid species, with or without a reference genome.

gene mappinggenome resequencinggenomic selectiongenotyping-by-sequencingRNA-seqSNP discoverytranscriptome assembly

Ellumigen provides AI-native sequencing analysis. Its Ellumigen Explorer product transforms raw sequencing and study data into AI-guided bioinformatics insight.

AI-guided insightsequencing analysis

Entovations bridges cutting-edge research and real-world agricultural innovation, empowering agricultural producers, researchers, and innovators by decoding insect biology and connecting multi-omics research with agricultural impact. The company offers consultation and project design, next-generation sequencing and data analysis, and molecular diagnostics and performance analysis.

consultation and project designgenomic profilingmolecular diagnosticsshort- and long-read DNA/RNA 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 Genomicschromatin accessibility analysisCLIA-certified, CAP-accredited testinggenome assembly and annotationIllumina sequencinglibrary preparationmethylation profilingmicrobiome analysisNanoStringOxford Nanopore TechnologiesPacBio SMRT sequencingRNA and DNA extractiontargeted sequencingwhole exome sequencingwhole genome sequencing

EuchroGene provides an AI agent-powered lab operations platform for life-science labs, delivered on each lab's own dedicated high-memory server. The platform includes bioinformatics analysis, study design, manuscript writing, a paper library, a signed lab notebook, sequence tools and collaboration, operated by asking an AI agent in plain language.

AI agents for design, analysis, writing and papersalignmentsBLASTcloningCRISPRdedicated server hostinggene databasegenome browser (JBrowse 2)GPU-accelerated analysesprimer designRNA-seqvariant analysis