Research Scientist
Hyderabad, Telangana
Job Description
Job Description
The Global Trait Discovery Informatics (GTDI) group located at the DuPont Knowledge Centre (DKC), Hyderabad, India is currently seeking applications for a highly...
CSIR - UNIT FOR RESEARCH AND DEVELOPMENT OF INFORMATION PRODUCTS (CSIR- URDIP)
Adv. No. URDIP/ 15/2015
Opportunity for young Bioinformatics Professionals to make a career in the area of Intellectual Property
CSIR has set up a Unit 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 Institute is working relentlessly on developing technologies for sustainable utilization of Himalayan bioresources, and in the area of tea, floriculture, bamboos and medicinal and aromatic plants. Looking at the mission of the Institute,the...
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...
Central University of South Bihar
(Established under Central Universities Act, 2009)
BIT Campus, PO: B.V. College,
Patna – 800 014 (Bihar)
Employment Notice No. CUSB / 27 / Faculty / 2015
Appointment for Faculty Positions Applications...
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...
Rajiv Gandhi Centre for Biotechnology (RGCB), Thiruvananthapuram
Job Code: 060815(10)Y
Jr Research Fellow Posts At Rajiv Gandhi Centre for Biotechnology
Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications to recruit on vacant...
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...