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RNA测序资料下载 

♦  A Global View of Cancer-Specific Transcript Variants by Subtractive Transcriptome-Wide Analysis.

♦  EpCAM and A-Fetoprotein Expression Defines Novel Prognostic Subtypes of Hepatocellular Carcinoma.

♦ Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases.

♦  Serum MicroRNA Signatures Identified in a Genome-Wide Serum MicroRNA Expression Profiling Predict Survival of Non-Small-Cell Lung Cancer.

♦  Transcriptome Sequencing to Detect Gene Fusions in Cancer .
 

癌症疾病测序资料下载

♦  Genome remodelling in a basal-like breast cancer metastasis and xenograft.

♦ Frequent Mutations of Chromatin Remodeling Gene ARID1A in Ovarian Clear Cell Carcinoma.

♦  A small-cell lung cancer genome with complex signatures of tobacco exposure. 
 

表观基因组学测序资料下载

♦  Genome-wide analysis of aberrant methylation in human breast cancer cells using methyl-DNA immunoprecipitation combined with high-throughput sequencing.

♦ A ChIP-seq defined genome-wide map of vitamin D receptor binding: Associations with disease and evolution.

♦ Aberrant chromatin at genes encoding stem cell regulators in human mixed-lineage leukemia.

♦  Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosus.

♦ Human DNA methylomes at base resolution show widespread epigenomic Differences.

♦ Nucleosome dynamics define transcriptional enhancers.

♦  The DNA Methylome of Human Peripheral Blood Mononuclear Cells. 
 

单基因病测序资料下载

♦  Targeted capture and massively parallel sequencing of 12 human exomes.

♦  Exome sequencing identifies the cause of a mendelian disorder.

♦  Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing.

♦  Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.

♦  Exome Sequencing, ANGPTL3 Mutations,and Familial Combined Hypolipidemia. 
 

复杂疾病测序资料下载

♦  Design of Association Studies with Pooled or Un-pooled Next-Generation Sequencing Data.

♦  Exome Sequencing, ANGPTL3 Mutations,and Familial Combined Hypolipidemia.

♦  Finding the missing heritability of complex diseases.

♦  Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants.

♦  Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude. 
 

宏基因组学测序资料下载

♦ A human gut microbial gene catalogue established by metagenomic sequencing

♦  Meta Genomics的DNA提取方法.