The amount of databases we bioinformatician deal are just HUGE … In such cases, we always need to check our server for free spaces etc. I planned this article to explains 2 simple commands that most bioinformatician want to know when they...
Prioritizing missense variants for further experimental investigation is a key challenge in current sequencing studies for exploring complex and Mendelian diseases. A large number of in silico tools have been employed for the task of...
Gautam Buddha University (GBU) Noida invites applications for the follow posts
2014 March Advertisement from Gautam Buddha University (GBU)
Junior Research Fellow (JRF)
No. of Positions: 01
Educational Qualifications:
Master degree in any...
DEPARTMENT OF MOLECULAR BIOLOGY & GENETIC ENGINEERING
COLLEGE OF BASIC SCIENCE AND HUMANITIES
G.B. PANT UNIVERSITY OF AGRICULTURE AND TECHNOLOGY
PANTNAGAR -263145, UTTARAKHAND
No. CBSH/MBGE/356
Subject: Advertisement for the award of...
github.com - Mix is a tool that combines two or more draft assemblies, without relying on a reference genome and has the goal to reduce contig fragmentation and thus speed-up genome finishing. The proposed algorithm builds an extension graph where vertices...
UNIVERSITY OF HYDERABAD SCHOOL OF LIFE SCIENCES
Applications are invited from qualified individuals for a JRF/SRF position (sponsored by DBT/DST) at Prof. Jagan Pongubala’s laboratory, University of Hyderabad. Dr. Pongubala’s laboratory is...
github.com - VcfR is an R package intended to allow easy manipulation and visualization of variant call format (VCF) data. Functions are provided to rapidly read from and write to VCF files. Once VCF data is read into R a parser function extracts matrices from...
ADVT. No. S/BIC/01/2014-15
Bose Institute, Kolkata, invites applications from Indian Citizens for ONE (01) temporary position of Junior Research Fellow in the DBT sponsored project entitled, “Centre of Excellance (CoE) in Bioinformatics at Bose...
The method used to isolate, enrich and sequence a sample will affect the composition of the sequencing data in terms of the types of RNA species represented and their relative abundances