Rahul Agarwal
I'm a Bioinformatician and Programmer
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Introduction of Epigenomics
By Rahul Agarwal 4633 days agowww.genome.gov - What is the epigenome? What does the epigenome do? What makes up the epigenome? Is the epigenome inherited? What is imprinting? Can the epigenome change? What makes the epigenome change? How do changes in the epigenome contribute to...Walk in interview for Research Associate, Studentship and Traineeship at BIF, NEHU, Tura Campus
BIOINFORMATICS INFRASTRUCTURE FACILITY (BIF) Department of RDAP North-Eastern Hil University, Tura Campus Tura-79402, Meghalaya Walk in interview for Research Associate, Studentship and Traineeship at BIF Applications are invited for the...Your stress/depression came from ancestor
By Rahul Agarwal 4423 days agoStress drives changes in the sperm microRNA which carry forward to later generationsAssistant Professor at GAUHATI UNIVERSITY, GUWAHATI
Advt. No.T/2014/4 Ref. No. GU/Estt/T/308(VI)/2014/6451-61 Applications are invited from the Indian citizens for five (5) teaching posts of Assistant Professor (Contractual) under various departments of Gauhati University. Details of the...
Alignment-free sequence comparison tools available for next-generation sequencing data analysis
Last updated 3140 days ago by Abhimanyu Singh Comments (1)kallisto Transcript abundance quantification from RNA-seq data (uses pseudoalignment for rapid determination of read compatibility with targets) Software (C++) https://pachterlab.github.io/kallisto/ Sailfish Estimation of isoform abundances...China University of Macau PhD Position 2015 in Bioinformatics, Computer Science
The Computational Biology and Bioinformatics Group at the University of Macau is inviting applications for PhD Position. Applicants will work on a research project focusing on the flexible receptor protein-ligand docking algorithms for...AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing
By BioStar 3096 days agosourceforge.net - AIRVF that works on flowgram, raw and mapped reads and called variants to reduce artifact-driven false variant calls. Tests on sequencing data of standard reference material showed up to ∼98% reduction of false variants when combined to...JNU Neuroscience/Systems Biology/Mathematical modeling JRF Vacancies
School of Computational and Integrative Sciences Jawaharlal Nehru University New Delhi 110067 Recruitment for Project Applications were invited from the citizens of India for filling up the following temporary position for the CSIR sponsored...Heap: a highly sensitive and accurate SNP detection tool for low-coverage high-throughput...
By Jit 2977 days agogithub.com - Heap, that enables robustly sensitive and accurate calling of SNPs, particularly with a low coverage NGS data, which must be aligned to the reference genome sequences in advance. To reduce false positive SNPs, Heap determines genotypes and calls...MECAT: fast mapping, error correction, and de novo assembly for single-molecule sequencing reads
By Rahul Nayak 2955 days agogithub.com - MECAT is an ultra-fast Mapping, Error Correction and de novo Assembly Tools for single molecula sequencing (SMRT) reads. MECAT employs novel alignment and error correction algorithms that are much more efficient than the state of art of aligners and...
