Job Description: Walk-in-interview for SRF, JRF posts at Junagadh Agricultural University
Junagadh Agricultural University has given a recruitment notification to fill the posts of Senior, Junior Research Fellows in the establishment.
Name...
Advertisement No. : R&C/CD/427/2015 ,Vacancy Code: 4271501
Project Fellow Bioinformatics recruitment in Indian Institute of Chemical Biology (IICB) purely temporary
Name of the Project: "Genomics and Informatics Solutions for...
github.com - Filtering on quality and/or read length, and optional trimming after passing filters.Reads from stdin, writes to stdout.
Intended to be used:
directly after fastq extraction
prior to mapping
in a stream between extraction and...
The Methods and Algorithms for Bioinformatics (MAB) team at the LIRMM (computer science, robotics and microelectronics laboratory at the CNRS & University of Montpellier, France) is looking for talented individuals to fill two postdoctoral...
github.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...
Agricultural Knowledge Management Unit
ICAR-INDIAN AGRICULTURAL RESEARCH INSTITUTE
L.B.S Building, Pusa Campus,
New Delhi-110012
Walk-in-Interview: 18th December 2015
DBT funded project: Distributed Information Centre under BTISnet...
github.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...
Applications are invited from suitable candidates for filling up the purely temporary positions of one Research Associate (RA) and one Junior Research Fellow (JRF) in the DBT Part-B Sub-project-1&2 entitled Transcriptome and epigenome diversity...
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...