Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Strand NGS is a biologist friendly NGS analysis tool that allows biologists to analy...tal testing. Dr. Suman holds a Ph.D in Molecular and Cell Biology from Indian Institute of Science, Bangalore. Prior...2277 days ago
Gap filling or Contigs extensions tools !
There are many tools to perform gap filling using Illumina short reads, for example "GapFiller: a de novo assembly...cs.toronto.edu/hapsembler/scarpa.html). See the PAGIT protocol: http://www.sanger.ac...2178 days ago
List of non-commercial NGS genotype-calling software
...type calling (bcftools) GATK http://www.broadinstitute.org/gsa/wiki/index.php/The...uires fine-scale linkage map QCall ftp://ftp.sanger.ac.uk/pub/rd/QCALL Multi-sam...can be generated using Margarita (http://www.sanger.ac.uk/resources/software/margari...2109 days ago
Bioinformatics in Africa:- Part 1
The Institut Pasteur de Côte d’Ivoire was cre...Monod, then Leading of the Pasteur institute of Paris. The ...available to the researchers of the institute and partners Long&...1203 days ago