BOL

NBFGR, Lucknow is recruiting Bioinformatics experts for the post of Research Associate Name of Position : Research Associate No of Post : One Desired candidate Profile : Candidate should be PhD in Bioinformatics or equivalent or Post-Graduation...

www.molgen.mpg.de - Ranbow is a haplotype assembler for polyploid genomes. It has been developed for the haplotype assembly of the hexaploid sweet potato genome, which is highly heterozygous. Ranbow can also be applied to other polyploid genomes. After a first phasing,...

Advertisement: Research Position in Computational Biology in the group of Shree P. Pandey Positions available in the area of NGS data analysis, bioinformatics, plant genomics Project Description: Projects involves high throughput analysis of data...

Bash Script source: https://gist.github.com/santhilalsubhash/367befcf5216be4b1fd9   Information: This script converts EnsEMBL GTF...

Bioinformatics Infrastructure Facility, Department of RDAP, NEHU vacancy of Research Associate Name of the Post: Research Associate No. of the Post: 01 One Age Limit: Max. 35 years Salary: Rs. 22000/- per month plus HRA Required Job...

github.com - nQuire provides a statistical framework to study organisms with intraspecific variation in ploidy. nQuire is likely to be useful in epidemiological studies of pathogens, artificial selection experiments, and for historical or ancient samples where...

The pacman package is an R package management tool that combines the functionality of base library related functions into intuitively named functions.

Applications are invited for the position of Project Assistant in Bio-IT centre at IBAB, Electronic city, Bengaluru. The successful candidate will work in the next-generation sequencing (NGS) facility to perform nucleic acid isolations, quality and...

F.No. 1(122)/2015-Admn. (CABin Project) Research Associate/Young Professional/SRF Zoology job vacancies in National Bureau of Fish Genetic Resources (NBFGR) Post Name: Research Associate (Computer Science/ Applications)...

github.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...