Refine by
Applications
- FluidFM for CRISPR cell line development Accelerate your CRISPR gene editing and cell line engineering
- Single-cell omics with Live-seq
- Mechanobiology and single-cell adhesion measurements with FluidFM
- FluidFM for Neuroscience Pattern, stimulate, inject into, and analyze single neurons
- FluidFM for Virology Study viral entry and replication on a single virion-single cell level
- Excitation-Contraction-Energy (ECE) Coupling Analysis for Cardiac Physiology
Genomics Services Available In Iran
98 services found
Manufactured by:Yourgene Health based inManchester, UNITED KINGDOM
At Yourgene Genomic Services we believe every patient can benefit from understanding their unique genomic ...
Manufactured by:Creative Biogene-Mitochondrial Research based inNY, NEW YORK (USA)
According to the research needs of global customers on mitochondrial dynamics, Creative Biogene has developed a series of technical service platforms for mitochondrial genome monitoring and analysis. Rely on mature, advanced technology and an experienced professional team to provide customers around the world with the most comprehensive mitochondrial research services to help you ...
by:DNAnexus, Inc. based inMountain View, CALIFORNIA (USA)
The xVantage Group provides fast, accurate, and cost-efficient reference-quality genome assembly services. As a bioinformatics partner, we will collaborate with you on complex assembly, structural variation analysis, and physical mapping to achieve complete and accurate views of all types of genomic ...
by:PierianDx based inCreve Coeur, MISSOURI (USA)
Standardize genomic reporting and quickly scale your variant review and sign-out capacity with our clinically trained team of 30+ variant scientists and medical experts led by our board-certified medical ...
Manufactured by:Foundation Medicine, Inc. based inCambridge, MASSACHUSETTS (USA)
Our genomic information knowledgebase is continuously evolving, informed by every clinical sample sequenced with Foundation Medicine’s comprehensive genomic profiling tests. You can also access a unique clinicogenomic data set through our partnership with Flatiron Health, a leading provider of clinical ...
by:Burning Rock Biotech Limited based inGuangzhou, CHINA
Burning Rock utilizes our own proprietary large-scale genomic dataset based on personalized analyses of Chinese cancer patients*, ntegrates the experience from multi-dimensional clinical/scientific research and published data, to provide a one-stop cancer genomic data solution for biopharma partners, aiming to speed up precision drug development and reduce the ...
Manufactured by:Eton Bioscience, Inc. based inSan Diego, CALIFORNIA (USA)
With this service, we can clone an insert of interest into the specific vector provided by you. Upon completion, we will provide you with 2-3µg of DNA, sequence verification, and visualization from gel electrophoresis. ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Whole genome sequencing (WGS) identifies almost all changes in a patient’s DNA by sequencing both the entire protein coding and the non-coding regions of the ...
by:Decipher Biosciences Inc. based inSan Diego, CALIFORNIA (USA)
Decipher Bladder is the only genomic subtyping tool available to physicians in the United States treating patients with locally advanced bladder ...
by:Lucence Health Inc. based inPalo Alto, CALIFORNIA (USA)
Tissue500™ is a comprehensive genomic profiling test that detects clinically relevant mutations in 572 genes to identify a patient’s unique cancer ...
by:Admera Health based inSouth Plainfield, NEW JERSEY (USA)
Discover Single Nucleotide Polymorphisms (SNPs), Copy Number Variation (CNV), and Structural Variation. Flexible sample type, including FFPE curls or slides, blood, saliva, etc. Scalable high throughput capability operating in CLIA-lab. Bioinformatic support including QC, Mapping, Markdup, BQSR, Germline Variant Analysis, and ...
by:Decipher Biosciences Inc. based inSan Diego, CALIFORNIA (USA)
Nearly a decade of research and clinical testing has resulted in the accumulation of more than 85,000 whole transcriptome tumor profiles. Decipher GRID (for Research Use Only) is a proprietary artificial intelligence platform and database generating genomic discoveries, catalyzing the development of new products, and collaborating to accelerate drug development and clinical ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
All current sequencing technologies support - Illumina, PacBio, Oxford Nanopore, 10x, Hi-C, Ion Torrent, and others. Igenbio scientists utilize a multitude of assembly strategies - denovo, reference based, hybrid, metagenomic, and others. Gene Annotation and Functional Assignments placing genes into their functional or metabolic context utilizing KEGG Pathways, Gene Ontology, and the ERGO ...
by:Igenbio, Inc. based inChicago, ILLINOIS (USA)
Both Long and short read platforms available such as Illumina, PacBio, and Oxford Nanopore. Proximity Ligation Hi-C Sequencing for Genome Scaffolding. CLIA-compliant whole genome sequencing available. Variety of coverage levels: 10x, 30x, ...
Manufactured by:Foundation Medicine, Inc. based inCambridge, MASSACHUSETTS (USA)
Discover tissue AND blood-based FDA-approved comprehensive genomic profiling testing for all solid tumors with FoundationOne®CDx and FoundationOne®Liquid CDx. In addition, FoundationOne®Heme is a laboratory developed test for hematologic malignancies, sarcomas, or solid tumors where fusion detection is desired. ...
Manufactured by:Sangamo Therapeutics based inBrisbane, CALIFORNIA (USA)
Our investment in world-class manufacturing capabilities gives us the advantage of greater control over timelines, quality and supply for our robust pipeline. We have a state-of-the-art cGMP AAV manufacturing facility and trusted CDMO partner that together will support Sangamo’s diverse pipeline now, and in the ...
Manufactured by:Epigentek Group Inc. based inFarmingdale, NEW YORK (USA)
Whole Genome Bisulfite Sequencing (WGBS) is a bisulfite sequencing method to detect in-depth DNA methylation across the entire genome, including methylation at CpG sites and less common non-CpG site such as CNG. WGBS is the gold standard for bisulfite based DNA methylation studies as the entire genome is sequenced with base-level detail into ...
by:Burning Rock Biotech Limited based inGuangzhou, CHINA
Cancer is a complicated disease caused by genetic variation. The genetic variation may deprive cells of the normal control function, leading to immortalization and cancer. And targeted drugs work well in cancer therapy, which can kill cancer cells that carry specific genes of variation. However, patients may differ from each other regarding the in vivo genetic variation. As a result, patients ...
by:Revvity Gene Delivery (formerly SIRION Biotech) based inHamburg, GERMANY
Revvity Omics is at the forefront of pioneering advancements in healthcare through our sponsored testing programs. Our focus is on both common and rare disorders, and our mission is to empower individuals, promote early diagnosis, and contribute to cutting-edge research that can help transform lives. We take pride in the impact we have made on the lives of countless ...
by:SeqOmics Biotechnology Ltd. based inMórahalom Csongrád, HUNGARY
Areas of Application; De novo sequencing (sequencing of species with unknown genome). Resequencing (sequencing of species with known reference genome e.g. phylogenetic classification of bacteria, the extremely Accurate identification of sequence variations and SNPs). Transcriptome analysis, gene-expression (RNA-Seq; Digital Gene Expression Profiling, DGEP, Whole ...