Sandip Samaddar

We don’t have enough information about this author to calculate their statistics. If you think this is an error let us know.
Learn More
Copy number variation (CNV) is a form of structural alteration in the mammalian DNA sequence, which are associated with many complex neurological diseases as well as cancer. The development of next generation sequencing (NGS) technology provides us a new dimension towards detection of genomic locations with copy number variations. Here we develop an(More)
  • 1