The focus of Dr. Singh’s research and teaching is on the molecular mechanistic basis for environmental carcinogen-induced genetic (DNA damage) and epigenetic changes, and susceptibility to human cancer development
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Bioinformatics Centre, Bose Institute vacancy of Research Associate / Senior Research Fellow
Location where with post of Research Associate / Senior Research Fellow is available:
Bioinformatics Centre, Bose Institute in Kolkata, West...
Bioinformatics Trainee
Eligibility : MSc
Location : Kolkata
Last Date : 28 Dec 2015
Hiring Process : Walk - In
University of Kalyani
Bioinformatics Trainee Job position in University of Kalyani
Number of Posts : 02
Qualification : M.Sc....
Focusing on understanding the molecular mechanisms that regulate mRNA translation, localization and stability and role of non-coding RNAs in this process. Up to 90% of human DNA is estimated to be transcribed into so called non-coding RNAs that are...
Research Associate Job vacancies in University of Pune on temporary basis
No. of Post : 01
Department : Science and Technology
Qualifications : Ph.D. with specialization in Bioinformatics/Machine Learning/ Mathematical Biology/...
www.broadinstitute.org - Spines
Spines is a collection of software tools, developed and used by the Vertebrate Genome Biology Group at the Broad Institute. It provides basic data structures for efficient data manipulation (mostly genomic sequences, alignments,...
github.com - HiCdat: a fast and easy-to-use Hi-C data analysis tool
HiCdat is easy-to-use and provides solutions starting from aligned reads up to in-depth analyses. Importantly, HiCdat is focussed on the analysis of larger structural features of chromosomes,...
hgdownload.cse.ucsc.edu - This directory contains Genome Browser and Blat application binaries built for standalone command-line use on various supported Linux and UNIX platforms. To determine which set of binaries to download, type "uname -a" on the command line to display...
The laboratory is focused on the discovery and analysis of structural variation (SVs) from genomic sequence data. As part of the 1000 Genomes Project and other endeavors, we have helped produce initial fine-scale maps using a variety of SV discovery...