Easy-to-use, no-code bioinformatics software for NGS data analysis

Biologist-Friendly Bioinformatics


SciDAP is a bioinformatics platform that allows NGS data analysis without a bioinformatician or any knowledge of coding. Built with open-source, transparent pipelines developed by experts in the field, SciDAP produces publication-ready results in hours not months, moving research forward faster.

feature 1
feature 1Open-Source Pipelines
feature 2
feature 2Results in Hours Not Months
feature 3
feature 3Publication-Ready Images
Trusted by Scientists at
University of California, DavisUniversity of MichiganTexas A&M UniversityNYUFox Chase Cancer CenterCincinnati Children's HospitalColumbia UniversityUniversity Texas SouthwesternUniversity of MissouriUC RiversideHarvard University

Easy to use

In just a few minutes, even the most novice user can start analyzing
NGS data with SciDAP. Here’s how:
Step 1
Start with just the raw FASTQ files.
right arrow
Step 2
Experiment type
Select the type of experiment (e.g., RNA-Seq), genome, and link FASTQ files.
right arrow
Step 3
Start analysis with a few clicks, without writing a single line of code.
right arrow
Step 4
Easily explore data, adjust analysis parameters.
right arrow
Step 5
Share data with lab members.
right arrow
Step 6
Create publication-ready images.
That’s it. SciDAP is so easy to use and saves so much time, now biologists can produce publication-ready results in hours not months.
all news