Alignment of Contigs and Reads to Reference Genome

With the help of Next Generation Sequencing (NGS) technologies large amount of data produced in form of small reads, read size may vary according to the technology used. Reads can be aligned on the reference genome with the help of several softwares.
By the use of several softwares for the assembling of reads we can generate long contigs.
Contigs produced should be aligned on a reference genome for several studies like gene prediction,noncoding RNA prediction,protein prediction etc.
Here we are providing the facility of both, Alignment of reads and Contigs as well.
We have used several softwares to make this platform user friendly.

We have collected all resources for the assembling of genomes also.
CRAG- Computational Resources for Assembling of Genomes.