Jit
Enthusiast computational biologist with business dream !!!
Our Sponsors
Related items
HALC: High throughput algorithm for long read error correction
By Jit 2982 days ago Comments (1)github.com - HALC, a high throughput algorithm for long read error correction. HALC aligns the long reads to short read contigs from the same species with a relatively low identity requirement so that a long read region can be aligned to at least one contig...National Institute of Biologicals Recruitment 2015
National Institute of Biologicals (NIB), Noida Job Code: 260415(04)Y National Institute of Biologicals (NIB), Noida invites applications to recruit on vacant posts of Scientist, Training Officer, Administrative Assistant, Stenographer, Junior...
Convert EnsEMBL GTF to Annotation table (Geneid, GeneSymbol, GeneWiseChrLocation, GeneClass,...
Last updated 2930 days ago by Jitendra NarayanBash Script source: https://gist.github.com/santhilalsubhash/367befcf5216be4b1fd9 Information: This script converts EnsEMBL GTF...Walk-ins for JRF ans SRF post in NIRRH, Mumbai
Title of project- "EXPLORING THE HINGE AND TRANSMEMBRANE REGION OF HUMAN FSHR FOR DESIGN OF SMALL MOLECULE AND PEPTIDOMIMETIC MODULATORS" Name of the Post- Junior Research Fellow No. of vacancy- One Stipend- Rs. 25000/ +30% HRA Essential...BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2849 days agogithub.com - new de novo assembler called BASE. It enhances the classic seed-extension approach by indexing the reads efficiently to generate adaptive seeds that have high probability to appear uniquely in the genome. Such seeds form the basis for BASE...JRF Bioinformatics @ Pune University
Pune University is inviting applications from indian citizens for recruiting following posts: Vacancies: Junior Research Fellow-04 Age Limits: Candidates age should be not more than 28 years. Qualification: Candidates should possess M.Sc in...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2745 days agogithub.com - nQuire implements a set of commands to estimate ploidy level of individuals from species, where recent polyploidization occurred and intraspecific ploidy variation is observed. Specifically, nQuire uses next-generation sequencing data to distinguish...Affy has acquired Eureka Genomics for 15M $
By Martin Jones 4096 days agoAffymetrix Acquires Assets Of Eureka Genomics CorporationClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 2394 days agogithub.com - ClinCNV detects CNVs in germline and somatic context in NGS data (targeted and whole-genome). We work in cohorts, so it makes sense to try ClinCNV if you have more than 10 samples (recommended amount - 40 since we estimate variances from...Alessandra Carbone Lab
Our group works on various problems connected with the functioning and evolution of biological systems. We use mathematical tools, coming from statistics and combinatorics, algorithmic tools and molecular physics tools to study basic principles of...
