Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Strand NGS is a biologist friendly NGS analysis tool that allows biologists to analyze their data using a very int...isease management and prenatal testing. Dr. Suman holds a Ph.D in Molecular and Cell...2262 days ago
Tools to Predict the Impact of Missense Variants !
Prioritizing missense variants for further experimental investigation is a key challenge in...ino acid substitution on the structure and function of a huma...variants as well as insertion/deletions variants in the human...2201 days ago
Gap filling or Contigs extensions tools !
There are many tools to perform gap filling using Illumina short reads, for example...om/landingpages/basetools-a-wide-range-of-bioinformatics-solutions/sspacev12/), ATLAS tools (http://www.hgsc.bcm.tm...2163 days ago
Bioinformatics tools for genome assembly !
There are numerous genome assembly tools available, each with its strengths and weaknesses. Here is a list of...September 2021: SPAdes: An assembler specifically designed for single-cell and multi-cell...284 days ago