genomics Downloads
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Saphyr - Whole Genome Imaging Instrument Brochure
Optical mapping with Genome Imaging using Saphyr reveals what’s missing in your research. Rapidly identify genome variation like never before with the high-throughput Saphyr ...
By Bionano
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High-throughput Transcriptome Sequencing Powered by Innovation and Expertise
CD Genomics provides a complete list of transcriptomics sequencing to meet the needs and budgets of our clients. Transcriptomic sequencing can be used for differential expression analysis, detection of mutations (SNPs/InDels), and functional annotation. This is a brief overview of our transcriptomic services. Visit https://www.cd-genomics.com/Transcriptomics.html for more facts. ...
By CD Genomics
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Genomic DNA - Brochure
301 Moved ...
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The Broad Prospects of miRNA Research
The use of the latest high-throughput technologies, such as miRNA microarrays and miRNA-Seq, allows further in-depth research on the mechanism by which miRNA functions. CD Genomics excels at providing a comprehensive portfolio of sequencing services. Our miRNA-Seq and miRNA microarray will help you study the role of miRNAs in cell differentiation, biological development, disease development, and ...
By CD Genomics
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Epigenomics at CD Genomics
CD Genomics provides a wide range of epigenomics sequencing services to meet the needs and budget of our clients. They can be used for many purposes, including detection of various methylations, elucidation of mechanisms of complex disease, disease diagnosis, and translational discovery. https://www.cd-genomics.com/Epigenomics.html ...
By CD Genomics
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Premium
BEC - Model SARS-CoV-2 RT - Lamp Kit brochure
BEC SARS-CoV-2 RT-LAMP system is designed for the rapid detection of SARS-CoV-2 genome on the field. It is composed of reagent kits and a dedicated reading instrument. The tests have been developed by Bertin Technologies and Enalees to allow a fast and easy molecular testing solution during the Covid-19 ...
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Sequencing Approach Enables More In-depth Phageome Investigation
CD Genomics, an advanced sequencing service provider equipped with extensive technologies and knowledge in phageome, is now ready to provide comprehensive Phage Genome Sequencing and Metagenomics Services. https://www.cd-genomics.com/Microbial-Whole-Genome-Sequencing.html ...
By CD Genomics
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Exploring Epigenomic Changes
CD Genomics provides a wide range of epigenomics sequencing services to meet the needs and budget of our clients. They can be used for many purposes, including detection of various methylations, elucidation of mechanisms of complex disease, disease diagnosis, and translational discovery. ...
By CD Genomics
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Gene Mutation and Expression Profiling
CD Genomics provides a complete list of transcriptomics sequencing to meet the needs and budget of our clients. Transcriptomic sequencing can be used for differential expression analysis, detection of mutations (SNPs/InDels), and functional annotation. This is a brief overview of our transcriptomic services. Visit https://www.cd-genomics.com/Transcriptomics.html for more facts. ...
By CD Genomics
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Genomic - Model µ-Grinder/µ-Sampler 96 - Varietal Molecular Plant - Brochure
The µ-Grinder 96 is a grinder developed to carry out varietal selection of plants by molecular markers from grains. It is characterized in particular by its pestle-mortar technique specially designed to grind plant matrices in very small ...
By Genomic SAS
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Broad Prospects of miRNA Research
The use of the latest high-throughput technologies such as miRNA microarray and miRNA-Seq allows further in-depth research on the mechanism of miRNA functions. CD Genomics excels in providing a comprehensive portfolio of sequencing services. Our miRNA-Seq and miRNA microarray will help you study the role of miRNAs in cell differentiation, biological development, disease development, and beyond. ...
By CD Genomics
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Lentiviral Integration Site Analysis
A lentiviral vector can be constructed and amplified to replace the transient expression vector. After the lentiviral vector clone is packaged, it can be used to infect cells that are difficult to transfect with traditional transfection reagents, such as primary cells, suspension cells, and cells in a nondividing state, and then integrated into the genome of infected cells for long-term stable ...
By CD Genomics
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10x-Genomics - Chromium Controller- Brochure
Single cell resolution to maximize biological ...
By 10x Genomics
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Genomic - Model Maxi-Grinder Solo - Grinder Homogeneizer - Brochure
Designed to strongly develop your laboratory by increasing productivity, ground remains quality and homogeneity while reducing costs. ...
By Genomic SAS
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CD Genomics Offers Advanced Solutions for Genomic, Transcriptomic, and Epigenetic Studies
To complement our SGS solutions, CD Genomics offers PacBio SMRT sequencing and Oxford Nanopore sequencing. We provide advanced solutions for genomic, transcriptomic, and epigenetic studies by utilizing long-read single-molecular sequencing. Our highly skilled and knowledgeable team can assist you with any procedure to ensure accurate and unbiased findings. ...
By CD Genomics
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10x-Genomics - Chromium Connect System - Brochure
Automate your single cell ...
By 10x Genomics
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The Time is Now for Bacteriophage Research
Sequencing technologies, genomics,and bioinformatics are rapid and effective tools to study phage genomics. In addition, further analysis,including transcription,translation, regulation, and modification, is also emerging as a technique that is extremely helpful in exploring the life cycle, specificity, lytic ability, and lysogenicity of phages. ...
By CD Genomics
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Case Studies of Gut Microbiome Sequencing
CD Genomics provides comprehensive high-throughput sequencing as well as reagents for general researchers. Using our Illumina, Nanopore, PacBio, 10x Genomics, and other mainstream service platforms, we provide sequencing services covering a variety of research directions in human, animal, plant, and microorganism. ...
By CD Genomics
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High-Throughput Genotyping Paves the Way in Genomics
Single-nucleotide polymorphisms (SNPs) are found in both coding and non-coding regions of genes, one of the most common types of variation; single nucleotide variants (SNVs) are characterized by changes in a single position within the DNA sequence, including conversions, reversals, insertions or deletions, with a variable frequency of >1%. In humans, approximately 3 ×10° SNPs were found, with an ...
By CD Genomics
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WGS, WES, and Targeted Gene Panels for Your Disease Research
As a company with innovative sequencing and genotyping technologies, CD Genomics uses the NGS Panel platform to provide a series of proprietary, ultra-high multiplexed target enrichment technology that integrates the company’s advanced panel design. The disease panels are designed to address the practical needs of various disease studies. ...
By CD Genomics
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