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Dianna Gellar

Marketing Manager at CD Genomics

United States · ShirleyJoined March 2016

Summary

CD Genomics aims to provide the research community with high-quality next-generation sequencing, PacBio SMRT sequencing, Oxford Nanopore sequencing, and microarray services. Due to increased demand for our services, CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. At present, our senior bioinformaticians have viewed more than 10,000 trace files and accumulated rich experience with our Illumina HiSeq X, Illumina MiSeq, PacBio Sequel II, Oxford Nanopore MinION, Oxford Nanopore PromethION, MGI DNBSEQ-G400, MGI DNBSEQ-T7, Illumina iScan, and Sequenom MassARRAY iPLEX Gold, etc. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs.
https://www.cd-genomics.com/

Research areas of interest (3)

  • Genetic Engineering Technology
  • Genome Research
  • Genetic Engineering Market

Dianna Gellar didn't publish any Technology Call yet

When classifying bacteria and fungi, morphological features are v¬ery relevant. Colony morphology is a useful tool widely used to classify and define them by researchers. Carefully studied and used during these experiments are the colony properties of individual bacterial and fungal colonies. Compar[…]

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Chimeric RNA, also known as fusion RNA, refers to RNA molecules that are formed as a result of the fusion of two or more different RNA transcripts. Chimeric RNA, a unique class of RNA molecules formed through various molecular mechanisms, such as trans-splicing, read-through transcription, and fusio[…]

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RNA modifications, not limited to purine or pyrimidine bases, including N6-methyladenosine (m6A), 1-methyladenosine (m1A), 5-methylcytidine (m5C), 5-hydroxymethylcytidine (hm5C), 5-formylcytidine (f5C), 5-carboxycytidine (ca5C), inosine (I), pseudouridine (Ψ), and 2′-O-methylation (Nm). RNA modifica[…]

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Amplicon sequencing is based on NGS technology or PacBio SMRT sequencing. The ultra-deep sequencing of amplicons (PCR products) allows efficient variant identification and characterization. This technique has a wide range of applications, including 16S/18S/ITS gene sequencing, SNP genotyping, CRISPR[…]

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