Results for "Chittaranjan National Cancer Institute"
Top-level pages
alignment: the mapping of a raw sequence read to a location within a reference genom...g and filtering genomics variants. Created by Heng Li, currently of the Broad Institute. single-read sequencing: seq...2882 days ago
Genome Assembly Tools and Software - PART1 !!
The genome assemblers generally take a file of short sequence reads and a file of qu...g Newbler Genome Assemblies. Gap Resolution was developed by DOE Joint Genome Institute to improve Newbler genome ass...2698 days ago
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
Some useful Bioinformatics links
Reference-free prediction of rearrangement breakpoint read...lery-of-nanoplot/ Tool documentation https://broadinstitute.github.io/picard/command-l...NA inverted repeats in the genome | Nature Reviews Cancer https://www.nature.com/articles...2254 days ago
Tools to Predict the Impact of Missense Variants !
Prioritizing missense variants for further experimental investigation is a key challenge in current sequencing stu...pact of amino acid substitutions in proteins, such as mutations discovered in cancer or...2216 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
- « Previous
- 1
- 2
- 3
- Next »
