Introduction
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About IGB
New sequencing technologies are making it much easier for labs to produce huge volumes of short- and long-read sequencing data. More mature genome-scale technologies, such as tiling arrays, continue to be used in many labs to interrogate At the same time, more labs are using tiling arrays to study expression patterns, identify sites bound by transcriptional factors, and explore the epigenome. To understand what these new data sets mean, researchers need to view their data alongside other known features of the genomic landscape.
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- View your RNA-Seq, ChIP-chip or ChIP-seq data alongside publicly-available genome annotations and sequence.
- Investigate alternative splicing, regulation of gene expression, epigenetic modifications of DNA, and other genome-scale questions.
- View results from aligning short-read sequences onto a target genome, identify SNPs, and check alignment quality.
- Copy genomic sequence for further analysis in other tools, such as primer design and promoter analysis tools.
- Create high-quality images for publication in a variety of formats, including PDF, PNG, and more.
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