genome-sequencing Downloads
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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. ...
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 ...
A deep learning-powered diagnostic application leveraging low-pass whole genome sequencing (WGS) to identify patterns of genomic instability in ovarian cancer samples. Supports accurate detection homologous recombination deficiency (HRD) status with the analytical capabilities and advanced features of the SOPHiA DDM™ ...
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. ...
CD Genomics is an innovative sequencing and genotyping company. Our cancer panels are designed to address the practical needs of cancer-related studies. ...
Sequencing-based genome editing validation can detect whether alleles of a gene have been edited correctly, identify insertion and deletion sites at the whole-genome level, and screen and identify monoclonal cell lines. In addition,it is an excellent way to study the off-target effects of CRISPR gene editing. ...
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. ...
CD Genomics is dedicated to providing a comprehensive list of genomics and microarray solutions for agriculture, including genome, exome, transcriptome, and metagenome sequencing, genome-wide association studies (GWAS), and targeted sequencing and genotyping that focus on a subset of regions or genes such as single nucleotide polymorphisms (SNPs). ...
CD Genomics is dedicated to providing a comprehensive list of genomics and microarray solutions for agriculture, including genome, exome, transcriptome, and metagenome sequencing, genome-wide association studies (GWAS), and targeted sequencing and genotyping that focus on a subset of regions or genes such as single nucleotide polymorphisms (SNPs). ...
CD Genomics is dedicated to providing a comprehensive list of genomics and microarray solutions for agriculture, including genome, exome, transcriptome, and metagenome sequencing, genome-wide association studies (GWAS), and targeted sequencing and genotyping that focus on a subset of regions or genes such as single nucleotide polymorphisms (SNPs). ...
CD Genomics offers several sequencing approaches using next-generation sequencing or long-read sequencing technologies to explore multiple types of genetic mutations in tumors, hence understanding the molecular mechanisms underlying carcinogenesis. ...
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, allowing a large number of cancer-related genes to be detected in a single assay. ...
CD Genomics's cancer panels are predesigned panels for targeted sequencing of genes and mutations associated with multiple cancer diseases. CD Genomics utilizes targeted NGS sequencing technology to provide more efficient and accurate targeting of specific genes or mutations, and even to detect low-frequency variations in cancer-associated genes. ...
To support medical research and translation, CD Genomics provides a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumour heterogeneity. ...
CD Genomics has global recognition for providing innovative and bespoke genome sequencing and microarray services and products to the life science industries and academic research institutions. We possess cutting-edge sequencing capabilities (i.e., NGS, Nanopore, Pacbio SMRT sequencing) and bioinformatics expertise. ...
Whole-Genome Sequencing can be used to determine which antibiotic resistance genes (ARGs) are present in microbial strains, discover novel ARGs, identify mobile genetic elements that promote the transfer of ARGs to other microorganisms and assess the safety of particular bacterial strains. https://www.cd-genomics.com/microbioseq/gene-expression-analysis.html ...
Based on rich experience in targeted sequencing, CD Genomics has developed a Disease Panel platform for targeted sequencing of disease-related genes to help researchers with cancer diagnostics and analysis, pathogen detection, and pharmacogenomics testing. ...
To support medical research and translation, we provide a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumor heterogeneity. ...
To support medical research and translation, CD Genomics provides a full range of sequencing/microarray-based approaches including gene expression profiling, RNA-seq, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenomics, and single-cell sequencing for detecting tumour heterogeneity. https://www.cd-genomics.com/Gene-Expression-Profiling-Microarray-Service.html ...
Sequencing-based genome editing validation can detect whether alleles of a gene have been edited correctly, identify insertion and deletion sites at the whole-genome level, as well as screen and identify monoclonal cell lines. In addition, it is an excellent way to study the off-target effects of CRISPR gene editing. NGS is a massively parallel sequencing strategy that allows for higher ...