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03/01/1990
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rna seq data analysis Créer$0.001En stock0 AperçuWe provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data analysis https://rna.cd-genomics.com/rna-sequencing.html
We provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data analysis https://rna.cd-genomics.com/rna-sequencing.html0 Commentaires 0 Parts 707 Vue 0 Aperçu -
atac sequencing Créer$100En stock0 AperçuAssays for Transposase-Accessible Chromatin using sequencing, short for ATAC-Seq, is a next-generation sequencing (NGS)-based method to study the open regions of chromatin on a genome-wide scale. ATAC-Seq has the advantages of easy operation, no crosslinking required, high signal-to-noise ratio, and low requirement for sample amount. Combined the data of ATAC-Seq, RNA-Seq, and epigenomics, the relationship between gene differential expression and regulation can be studied more accurately and comprehensively. atac sequencing https://rna.cd-genomics.com/atac-sequencing.html
Assays for Transposase-Accessible Chromatin using sequencing, short for ATAC-Seq, is a next-generation sequencing (NGS)-based method to study the open regions of chromatin on a genome-wide scale. ATAC-Seq has the advantages of easy operation, no crosslinking required, high signal-to-noise ratio, and low requirement for sample amount. Combined the data of ATAC-Seq, RNA-Seq, and epigenomics, the relationship between gene differential expression and regulation can be studied more accurately and comprehensively. atac sequencing https://rna.cd-genomics.com/atac-sequencing.html0 Commentaires 0 Parts 549 Vue 0 Aperçu -
single cell seq Créer$100En stock0 AperçuSingle-cell RNA sequencing (scRNA-seq) is a next-generation sequencing (NGS)-based method to amplify and sequence the whole transcriptome of a single cell. It is becoming a powerful tool and has been applied to research related to stem cell differentiation, embryogenesis, whole tissue analysis, and even tumors. single cell seq https://rna.cd-genomics.com/single-cell-rna-seq.html
Single-cell RNA sequencing (scRNA-seq) is a next-generation sequencing (NGS)-based method to amplify and sequence the whole transcriptome of a single cell. It is becoming a powerful tool and has been applied to research related to stem cell differentiation, embryogenesis, whole tissue analysis, and even tumors. single cell seq https://rna.cd-genomics.com/single-cell-rna-seq.html0 Commentaires 0 Parts 584 Vue 0 Aperçu -
rna seq data Créer$100En stock0 AperçuWe provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data https://rna.cd-genomics.com/rna-sequencing.html
We provide a full range of RNA sequencing services to help analyze the gene expression patterns, examine changes in the transcriptome, and detect novel RNA molecules, mutations, and gene fusions, enabling a deeper understanding of RNA biology and disease development. In addition to NGS, we provide a long-read sequencing-based method (iso-seq) for full-length transcript sequencing, avoiding errors that can occur with NGS approaches. rna seq data https://rna.cd-genomics.com/rna-sequencing.html0 Commentaires 0 Parts 1KB Vue 0 Aperçu -
microseq microbial identification system Créer$0.001En stock0 AperçuWe provide MicroSEQ® microbial identification service based on sequencing of the 16S rRNA gene and ITS/D2 region of 28S large subunit (LSU) rRNA gene to identify the microbial species. microseq microbial identification system https://www.cd-genomics.com/microbioseq/microseq-microbial-identification.html
We provide MicroSEQ® microbial identification service based on sequencing of the 16S rRNA gene and ITS/D2 region of 28S large subunit (LSU) rRNA gene to identify the microbial species. microseq microbial identification system https://www.cd-genomics.com/microbioseq/microseq-microbial-identification.html0 Commentaires 0 Parts 702 Vue 0 Aperçu -
smrt sequencing disadvantages Créer$100En stock0 AperçuPacbio SMRT sequencing technology can sequence a single molecule DNA in real time without amplification, and generates kilobase-long reads with the potential to complete microbial genome assembly. smrt sequencing disadvantages https://www.cd-genomics.com/microbioseq/pacbio-smrt-sequencing.html
Pacbio SMRT sequencing technology can sequence a single molecule DNA in real time without amplification, and generates kilobase-long reads with the potential to complete microbial genome assembly. smrt sequencing disadvantages https://www.cd-genomics.com/microbioseq/pacbio-smrt-sequencing.html0 Commentaires 0 Parts 548 Vue 0 Aperçu -
nanopore dna methylation Créer$100En stock0 AperçuWe offer professional microbial epigenomics service to analyze the frequency and distribution of methylated residues in microbial genomes for a full understanding of their functions by using Nanopore sequencing technologies. nanopore dna methylation https://www.cd-genomics.com/microbioseq/nanopore-based-microbial-epigenomics.html
We offer professional microbial epigenomics service to analyze the frequency and distribution of methylated residues in microbial genomes for a full understanding of their functions by using Nanopore sequencing technologies. nanopore dna methylation https://www.cd-genomics.com/microbioseq/nanopore-based-microbial-epigenomics.html0 Commentaires 0 Parts 558 Vue 0 Aperçu -
smrt transcriptomic sequencing Créer$100En stock0 AperçuWe provide professional SMRT-based transcriptomics analysis service to identify novel transcript isoforms, fusion gene expression and alternative splicing events, and improve genome annotation. smrt transcriptomic sequencing https://www.cd-genomics.com/microbioseq/smrt-based-transcriptomics-analysis.html
We provide professional SMRT-based transcriptomics analysis service to identify novel transcript isoforms, fusion gene expression and alternative splicing events, and improve genome annotation. smrt transcriptomic sequencing https://www.cd-genomics.com/microbioseq/smrt-based-transcriptomics-analysis.html0 Commentaires 0 Parts 538 Vue 0 Aperçu -
rna seq analysis Créer$100En stock0 AperçuCD Genomics is a provider of transcriptome bioinformatic data analysis. We can analyze transcriptome raw data of different sequencing platforms, different samples, and different sequencing depths, maximizing the mining of data information. rna seq analysis https://bioinfo.cd-genomics.com/transcriptomics.html
CD Genomics is a provider of transcriptome bioinformatic data analysis. We can analyze transcriptome raw data of different sequencing platforms, different samples, and different sequencing depths, maximizing the mining of data information. rna seq analysis https://bioinfo.cd-genomics.com/transcriptomics.html0 Commentaires 0 Parts 534 Vue 0 Aperçu -
ngs data analysis Créer$100En stock0 AperçuThe concept of genomics (genomics) was first proposed by American geneticist Thomas H. Roderick in 1986. Genomics is a cross-biological subject that implements collective characterization, quantitative study and comparative study of different genomes of all genes in organisms. The structure, function, evolution, location, editing and their effects on organisms of genomes can be studied by bioinformatics. ngs data analysis https://bioinfo.cd-genomics.com/genomics.html
The concept of genomics (genomics) was first proposed by American geneticist Thomas H. Roderick in 1986. Genomics is a cross-biological subject that implements collective characterization, quantitative study and comparative study of different genomes of all genes in organisms. The structure, function, evolution, location, editing and their effects on organisms of genomes can be studied by bioinformatics. ngs data analysis https://bioinfo.cd-genomics.com/genomics.html0 Commentaires 0 Parts 508 Vue 0 Aperçu -
chip seq analysis Créer$100En stock0 AperçuAs a leading provider of ChIP-Seq data analysis, CD Genomics uses bioinformatics to help you decode the mystery of protein and DNA binding. Our unique data analysis skill set combined with the most advanced software tools will meet clients' needs for personalized laboratory data analysis and provide the easy-to-interpret data analysis reports. chip seq analysis https://bioinfo.cd-genomics.com/chip-seq-analysis.html
As a leading provider of ChIP-Seq data analysis, CD Genomics uses bioinformatics to help you decode the mystery of protein and DNA binding. Our unique data analysis skill set combined with the most advanced software tools will meet clients' needs for personalized laboratory data analysis and provide the easy-to-interpret data analysis reports. chip seq analysis https://bioinfo.cd-genomics.com/chip-seq-analysis.html0 Commentaires 0 Parts 229 Vue 0 Aperçu -
18s gene Créer$100En stock0 AperçuAs one of the leading providers of 16S/18S/ITS amplicon sequencing data analysis, CD Genomics uses bioinformatics to help you detect the diversified environmental microorganisms in one step. Our unique data analysis platform can also meet customers' personalized data analysis needs and provide you with a fast analysis cycle and a high-quality result report. 18s gene https://bioinfo.cd-genomics.com/16s-18s-its-amplicon-sequencing.html
As one of the leading providers of 16S/18S/ITS amplicon sequencing data analysis, CD Genomics uses bioinformatics to help you detect the diversified environmental microorganisms in one step. Our unique data analysis platform can also meet customers' personalized data analysis needs and provide you with a fast analysis cycle and a high-quality result report. 18s gene https://bioinfo.cd-genomics.com/16s-18s-its-amplicon-sequencing.html0 Commentaires 0 Parts 248 Vue 0 Aperçu -
microsatellite analysis Créer$100En stock0 AperçuCD Genomics has extensive experience in providing support for the selection and design of microsatellite markers for a wide range of plant and animal species. Besides microsatellite genotyping, we also provide genotyping by sequencing (GBS) method, which saves time and resources. microsatellite analysis https://www.cd-genomics.com/Microsatellite-Genotyping-Service.html
CD Genomics has extensive experience in providing support for the selection and design of microsatellite markers for a wide range of plant and animal species. Besides microsatellite genotyping, we also provide genotyping by sequencing (GBS) method, which saves time and resources. microsatellite analysis https://www.cd-genomics.com/Microsatellite-Genotyping-Service.html0 Commentaires 0 Parts 266 Vue 0 Aperçu -
snp array testing Créer$100En stock0 AperçuCD Genomics is providing PacBio SMRT sequencing to complement our NGS facility. By taking advantage of the long-read and single molecular sequencing capability developed by PacBio, we are proud to offer advanced genome de novo assembly solutions and full-length gene/transcript sequencing strategy to suit your project needs. snp array testing https://www.cd-genomics.com/SNP-Microarray.html
CD Genomics is providing PacBio SMRT sequencing to complement our NGS facility. By taking advantage of the long-read and single molecular sequencing capability developed by PacBio, we are proud to offer advanced genome de novo assembly solutions and full-length gene/transcript sequencing strategy to suit your project needs. snp array testing https://www.cd-genomics.com/SNP-Microarray.html0 Commentaires 0 Parts 187 Vue 0 Aperçu -
snp genotyping Créer$100En stock0 AperçuCD Genomics provides the whole-genome SNP genotyping for the overview of the entire genome by using both microarray technologies and high-throughput next-generation sequencing (NGS), enabling genome-wide discoveries and screening of the SNP loci. Genome-wide association studies with SNP markers are expected to allow identification of genetic variation that underlie complex disorders. snp genotyping https://www.cd-genomics.com/Whole-Genome-SNP-Genotyping.html
CD Genomics provides the whole-genome SNP genotyping for the overview of the entire genome by using both microarray technologies and high-throughput next-generation sequencing (NGS), enabling genome-wide discoveries and screening of the SNP loci. Genome-wide association studies with SNP markers are expected to allow identification of genetic variation that underlie complex disorders. snp genotyping https://www.cd-genomics.com/Whole-Genome-SNP-Genotyping.html0 Commentaires 0 Parts 198 Vue 0 Aperçu
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