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The use of long-read sequencing technologies has risen dramatically as sequencing costs have decreased and accuracy and throughput have continued to advance. CD Genomics is a leading global life sciences company. We specialize in the application of long-read sequencing technologies, including Oxford Nanopore and PacBio SMRT sequencing. Here, we are providing long-read sequencing data analysis in a wide range of fields such as whole-genome sequencing, RNA sequencing, epigenetics, and so on. Since long-read sequencing data analysis is a rapidly developing and advancing research area. Our data analysis uses the latest algorithms to provide a tailored solution to your specific application needs.
Typically, long-read sequencing data analysis is a complex, computationally intensive, multi-step process that requires a high level of bioinformatics expertise. Each step in the analysis often requires a different set of tools or software. And some tools need significant computational resources, further adding to the complexity of the analysis process. As of early 2020, there are approximately 354 analytic tools for long-read data presented in publications (including preprints), social media, and online repositories. Among them, 262 tools are developed for performing Nanopore read analysis and 170 are SMRT data analysis tools. According to their functions, these tools can be divided into 31 groups, among which the more concerned and top-ranked are error correction polishing, de novo assembly, SNP and variant analysis.
We are committed to offering a flexible data analysis platform with diverse applications, including but not limited to the following:
Fig 2. Typical long-read analysis pipelines for SMRT and nanopore data. (Amarasinghe, S. L., et al., 2020)
Our long-read sequencing analysis platforms have integrated a series of long-read sequence tools. Please feel free to contact us for more information. We are glad to cooperate with you!