Comparative Sequencing Analysis Platform

CoSAP is an easy yet comprehensive pipeline creation tool for NGS data. It provides reproducibility and aims to give deeper insight about the powers and limitations of the current tools by allowing users to compare results of different pipelines.

A typical variant calling pipeline consists of Read Trimming, Read Mapping, Duplicate Removal&Base Calibration, Variant Calling and Variant Annotation steps. CoSAP provides several tool options for each of these steps.

You can access the GitHub page of cosap via this link.

CoSAP is also a program with a web interface. You can perform genomic analyzes using the web interface. Click to access the CoSAP website. CoSAP has a well-written document, you can access it from this link.