How it works:
1. FASTA files parser
You can upload
existing FATSA-file with DNA sequences or
select Refseq genome
and study overall statistics
for various properties such as GC-content, CpG-Islands, sequence length etc. Moreover,
you can apply filters on each of that properties or their combination to see how it affects on other properties.
2. Numerics parser
We have created some basic parser for numeric values, for example, if you have files with expression data,
you can upload
them to our server and then watch for statistics and apply filters to select values
by number range.
3. Combination of numbers and sequences
If your data can be merged with DNA sequences (for example, by their transcript ID), you can create a new project with all
the needed files uploaded to study wether there may be difference of properties based on filter applied.
You will be able to create and save subsets based on different filters and then compare how properties are distributed for each of them.