Shirley, NY--CD Genomics has worked relentlessly in applying NGS to FFPE samples. On the GenSeqTM Technology, expression data from RNA purified from FFPE samples is highly correlated with data from RNA matched fresh samples. Furthermore, the capability of CD Genomics make FFPE Samples Sequencing ideal for various types of clinical research studies and signature development, especially in cancer research. Millions of archival FFPE samples provide an enormous and invaluable repository of information for genotyping studies. These samples hold a wealth of data for biomarker discovery, drug development, and cancer research. However, formidable challenging to get intact information from such samples, as severe degradation, or chemical modification could occur during sample preparation and store process. There are quite few usages of next generation sequencing (NGS) method in deciphering the FFPE nucleotide information. To overcome this problem, the FFPE sample restoration solution provides a simple workflow to QC samples, repair damaged DNA, and achieve high-quality data. Benefits of FFPE Samples Sequencing Low input: As low as 200ng as for WGS, WES and RNA-Seq. High throughput: Millions of reads product for downstream analysis. Special analysis: Bioinformatics contents only for cancer tissue. About CD Genomics The professional scientist team of CD Genomics is committed to develop the present techniques to meet more scientific needs. The major services include sequencing, microarray, custom libraries, bioinformatics, genotyping, and aptamers, etc. More break through will come into the stage in the near future of CD Genomics. For more information, you can contact CD Genomics at info@cd-genomics.com or visit website http://www.cd-genomics.com.
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