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Deep Analysis for Deep-Sequencing of Cancer Genome

Led by internationally recognized cancer biologists, oncologists, and cancer informatics scientists, Genomic Future provides our customers with cancer genome/transcriptome deep-sequencing and deep analysis using a seamlessly integrated cancer informatics workflow from raw sequence data to biologically meaningful hypotheses and discoveries on driver mutations, biomarkers, therapeutic targets, and drug repositioning.

 Recent OncoDecoder Blog Posts

arrow Frequently Asked Questions in Cancer Research That Frame the
OncoDecoder Analysis Pipelines
arrow Challenge about Cancer Genome Analysis

What we offer:

Genome/transcriptome deep sequencing
Mutation detection and analysis
CNV and SNVs detection and analysis
RNA-Seq expression analysis
Small RNA-Seq analysis
Methylation analysis
Pathway analysis
Cross-tumor comparison analysis
Clinical correlation analysis

White Paper, Case Study & Research Report:

White Paper: OncoDecoder: The First Comprehensive NextGen Data Deep Analysis bioinformatics Workbench for Human Cancer Research
Case Study: Whole Exome Sequencing of Human Melanoma Reveals Important Gene Mutations
Research Report: OncoDecoder SNP/Indels Detection Makes Difference From Sequencing Vendor's Variant Data
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