2020-04-22 11:28 2D western blot is an effective and widely used technique for proteomic and biopharmaceutical analysis. This technique separates proteins according to two different properties and thus thousands of different proteins can be separated in one assay. 3D... дальше
2020-04-07 16:12 CD Genomics has extensive experience in offering Iso-Seq service by producing full-length transcripts without assembly. Strict quality control following every procedure is executed to ensure comprehensive and accurate results.
2020-04-07 16:12 CD Genomics provides fungal whole genome sequencing with the PacBio Sequel system to offer more insights into genetic structure and functions. We are best in the knowledge, practice, and experience.
2020-04-07 16:11 CD Genomics is providing PacBio Single Molecular Real-Time (SMRT) sequencing to increase your research method for bacterial whole genome sequencing. A comprehensive view of the bacterial genome, including genes, regulatory regions, IS elements, phage ... дальше
2020-04-07 16:11 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 ... дальше
2020-04-07 16:11 CD genomics combines proven ribosomal reduction library preparation chemistries and illumina NGS technology into a single, streamlined protocol. Ribo-Zero ribosomal RNA reduction chemistry minimizes ribosomal contamination and maximizes the percentag ... дальше
2020-04-07 16:11 Available on both Illumina and PacBio Platforms, CD Genomics offers the accurate and affordable mitochondrial DNA sequencing solution you’re looking for.
2020-04-07 16:10 CD Genomics provides complete plasmid DNA sequencing service, and our improved bioinformatics pipelines are available to perform de novo assembly with no reference required.
2020-04-07 16:10 CD Genomics provides statistical and bioinformatic data analysis services that help our customers to explain large amounts of data generated by sequencing, genotyping, and microarray experiments.