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1 Introduction 1.1 Intended use The smart DNA prep (m) kit has been designed for the manual isolation of high molecular weight genomic DNA (200 kb - > 500 kb) from tissue samples, eukaryotic cells, rodent tails, bacteria and ...
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1 Introduction 1.1 Intended use The smart Blood DNA Midi prep (m) has been designed for manual isolation of high molecular weight genomic DNA from peripheral blood mononuclear cells (PBMC) derived from fresh or frozen blood stabilized with EDTA, citrate or heparin. ...
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Malignant tumors exhibit abnormal DNA methylation - following a pattern differing significantly from that of healthy tissue - at a very early stage in tumorigenesis and during tumor progression. In general, genome-wide methylation in tumor cells decreases (genome-wide hypomethylation), while individual genes are hypermeth-ylated (gene-specific hypermethylation). ...
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This application note describes the successful proof of principle to generate high-quality DNA libraries on CyBi-FeliX for personal genome analysis with the Ion Torrent™ Sequencing ...
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1 Introduction 1.1 Intended use The kit has been designed as a tool for very fast and efficient isolation of genomic DNA from small amounts of different types of forensic samples like, hairs or hair roots; stains of blood, saliva or sperm; finger nails; cigarette butts; bubble gum; buccal swabs; stamps and envelopes as well as fingerprints on different surfaces. ...
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1. INTRODUCTION Analytik Jena's blackPREP FFPE DNA Kit is optimized for DNA extraction from a variety of FFPE (formalin-fixed, paraffin-embedded) tissue sample, e.g. adipose tissue, pancreatic tissue or placenta as starting ...
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 ...
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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. ...
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 ...
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 ...
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. ...
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. ...
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 ...
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 ...
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. ...
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. ...
Single cell resolution to maximize biological ...
Automate your single cell ...
Cancer is primarily caused by genetic alterations, which may be inherited or acquired in somatic cells. These alterations in oncogenes, tumour suppressor genes or DNA repair genes may enable cells to evade growth inhibition in response to growth-inhibitory signals, leading to the development of a ...
CD Genomics is an innovative sequencing and genotyping company. Our cancer panels are designed to address the practical needs of cancer-related studies. These panels are featured an innovative background cleaning technique that allows plenty of amplicons to be multiplexed in a single reaction pool. ...