Talks in this Session:
- Noninvasive prenatal diagnosis using fetal DNA in maternal plasma: from digital PCR to next-generation sequencing
- Qualitative and Quantitative Analysis of RNA by SOLiD Next Generation Sequencing
- Analysis of circulating nucleic acids (CNA) using NGS technologies
- Improved library quantification for High Throughput Sequencing at the Wellcome Trust of Human Genetics Oxford
- Application of the Next Generation Sequencing Technologies at JCVI
- The use of qRT-PCR and high-throughput transcriptomics for biomarker development
- Deep sequencing as diagnostic tool for highly pathogenic viruses
- High Resolution Transcription Profiling using Next-Generation-Sequencing identifies Diagnostic Markers for Malignancy
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