Dianna Gellar

Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:57:29 -

rna seq data analysis Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:56:59 -

atac sequencing Новое

$100

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:56:40 -

single cell seq Новое

$100

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:56:21 -

rna seq data Новое

$100

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:56:03 -

microseq microbial identification system Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 03:55:38 -

smrt sequencing disadvantages Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:08:00 -

nanopore dna methylation Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:07:40 -

smrt transcriptomic sequencing Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:07:21 -

rna seq analysis Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:07:03 -

ngs data analysis Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:06:44 -

chip seq analysis Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:06:24 -

18s gene Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:06:06 -

microsatellite analysis Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:05:45 -

snp array testing Новое

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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.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.html

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Dianna Gellar добавлен новый продукт для продажи
2022-04-14 02:05:27 -

snp genotyping Новое

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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.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.html

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