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Advt. No. AUMLR/BIF/ RA /6-2016 Research Assistant Job Position in Andhra University on temporary basis No. of Post : 01 Eligibility : Applicants who have completed their Post Graduate degree in Bioinformatics. Desirable : Undergone...

Applications are invited for: ICGEB NEW DELHI, INDIA Biotechnology research positions Projects include: a) protein structure determination b) malaria parasite biology c) genomics and metagenomics d) molecular and cellular biology e)...

Aravind J Shankar, a bioinformatics graduate of SASTRA University, has secured the all India rank 1 in BINC

Cas9 restricts DNA at specific Protospacer Adjacent Motifs (PAMs), which is species-dependent (for example, 5′ NGG 3′ for Streptococcus pyogenes Cas9).

No. RGCB/ADVT/ADMN&TECH/01/2016 August 17, 2016 RGCB invites applications for the following positions from Indian citizens with prescribed qualifications. Full details including job description, additional desirable qualifications, etc....

Scientist Advanced Centre for Treatment, Research and Education in Cancer - Navi Mumbai, Maharashtra Scientist (One position) Project: Bioinformatics centre DBT- Sub-DIC at ACTREC Funding agency: DBT Grant No.232 Duration of the Project:...

Bioinformatics center Sri Venkateswara College (University of Delhi) New Delhi- 110021 1. Junior Research Fellow (1 Post) Applications are invited for the post of Junior Research Fellow (JRF) under DST funded project which is purely...

decipher.cee.wisc.edu - DECIPHER is a software toolset that can be used to maintain, analyze, and decipher large amounts of DNA sequence data. To install DECIPHER, see the Downloads page. To begin using DECIPHER read the "Getting Started DECIPHERing" tutorial. Refer to the...

cancer.sanger.ac.uk - The accurate description and annotation of structural variants can be complex.  This is due to the different resolution that variants are reported from traditional cytogenetic coordinates down to the actual base pair positions....

mathgen.stats.ox.ac.uk - IMPUTE2 is a computer program for phasing observed genotypes and imputing missing genotypes. Most people use just a couple of the program's basic functions, but we have also built up a collection of specialized and powerful options. If you are...