As a Bioinformatician/ Computational biologist we swim in the ocean of genomic/proteomics data, and play with them with an ease. In our day to day simulation, analysis, comparative study we do need to run exhaustive programs, which might take more...
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...
lbbe.univ-lyon1.fr - The software package SiLiX implements an ultra-efficient algorithm for the clustering of homologous sequences, based on single transitive links (single linkage) with alignment coverage constraints.
SiLiX adopts a graph-theoretical framework to...
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...
github.com - lordFAST is a sensitive tool for mapping long reads with high error rates. lordFAST is specially designed for aligning reads from PacBio sequencing technology but provides the user the ability to change alignment parameters depending on the reads...
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...
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...
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...
github.com - HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). Based on an extension of BWT for...