LnRNA Research Experience:
Large –scale gene sequencing and Genomics/Epigeneomics:
I established multiple myeloid- specific cDNA libraries, and sequenced around 2,200 ESTs using 96-well format plates via Sanger sequencing. I also finished three CHIP-seq projects using NGS sequencing (Illumina), and one CHIP-seq project NGS sequencing for determine 6mdA modification using single molecule/real time sequencing (SMRTTM) technique. During my genome-wide studies, I analyzed high-throughput data using “ChIPpeakAnno” to annotate CHIP-seq data of DNA; using “Basespace”, “TopHat and Cufflinks” to analyze the RNA seq. data. (Blood, 2002, 100:833-844). (two manuscripts are under preparation).
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