Jit
Enthusiast computational biologist with business dream !!!
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FiNGS: Filters for Next Generation Sequencing
By Neel 2051 days agogithub.com - Key features Filters SNVs from any variant caller to remove false positives Calculates metrics based on BAM files and provides filtering not possible with other tools Fully user-configurable filtering (including which filters to use and their...Five key traits to seek out in potential bioinformatics candidates !!!
By Jit 4079 days agoOnce your research group is ready to make a larger investment and hire a bioinformatician to gain a competitive edge, there are several key traits to seek out in potential candidates. The best bioinformatician are:-
Libraries or management tools for high throughput sequencing data
Last updated 736 days ago by LEGEGATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.These methods enable the analysis of data sets of any size on multi-core desktop...JRF in Bioinformatics @ Central University of Rajasthan
Central University of Rajasthan Department of Biotechnology School of Life Sciences Bandarsindri, Distt. Ajmer Applications are invited for one JRF position supported by DST sponsored project in Bioinformatics with Dr. Tarun Kumar...1mb long DNA with Nanopore technology
By Jit 3216 days agoLongest read of 1mb achievements with NanoporeBioinformatics Training Fellowship !!
Applications are invited from suitable candidates for six months ‘Training Fellowship’ in Bioinformatics under the BTISNET program of DBT in the Distributed Information Sub center (DISC) facility at NIPGR, New Delhi, under the supervision of Dr....NanoPack: visualizing and processing long-read sequencing data
By Jit 2845 days agogithub.com - The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible...Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 2447 days agogithub.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...RA Bioinformatics at University of Delhi
BIOINFORMATICS INFRASTRUCTURE FACILITY GARGI COLLEGE (University of Delhi) SiriFort Road, New Delhi-110049 Walk- in- interview Bioinformatics Infrastructure Facility (BIF), Gargi College, University of Delhi invites to appear for interview...GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
By Jit 3412 days agogithub.com - GraphMap - A highly sensitive and accurate mapper for long, error-prone reads http://www.nature.com/ncomms/2016/160415/ncomms11307/full/ncomms11307.htmlFeatures Mapping position agnostic to alignment parameters. ...
