Rahul Agarwal
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Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By Rahul Nayak 2653 days agogithub.com - Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The...
A guide for complete R beginners :- R Syntax
Last updated 4245 days ago by Archana MalhotraR is a functional based language, the inputs to a function, including options, are in brackets. Note that all dat and options are separated by a comma Function(data, options) Even quit is a function q() So is...ngs-bits - Short-read sequencing tools
By Neel 2458 days agogithub.com - Binaries of ngs-bits are available via Bioconda. Alternatively, ngs-bits can be built from sources: Binaries for Linux/macOS From sources for Linux/macOS From sources for WindowsAsst. Professor at Central University of Jharkhand (CUJ)
Central University of Jharkhand (CUJ) has issued a recruitment notification for the recruitment of Assistant Professor through recruitment notification – Central University of Jharkhand (CUJ) Recruitment 2015 – Advt. No.: CUJ/Advt./14-15/15 Date:...HASLR: a tool for rapid genome assembly of long sequencing reads
By LEGE 2444 days agogithub.com - HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires long reads generated by Third Generation Sequencing technologies (such as PacBio or Oxford Nanopore) together with Next Generation...RA Bioinformatics at Ch. Charan Singh University, Meerut
Ch. Charan Singh University, Meerut http://molbiolabccsumrt.webs.com/ Applications are invited for one post of RA in a DBT funded research project “Creation of Bioinformatics Infrastructure Facility (BIF) for the promotion of Biology Teaching...Parliament2: Runs a combination of tools to generate structural variant calls on whole-genome...
By Jit 2325 days agogithub.com - Parliament2 identifies structural variants in a given sample relative to a reference genome. These structural variants cover large deletion events that are called as Deletions of a region, Insertions of a sequence into a region, Duplications of a...Coding Ground
By Jitendra Narayan 4225 days agowww.tutorialspoint.com - Online coding group for most of the programming languages. Code in almost all popular languages using Coding Ground. Edit, compile, execute and share your projects, 100% cloud. http://www.tutorialspoint.com/codingground.htmSmudgeplot: Inference of ploidy and heterozygosity structure using whole genome sequencing data
By Neel 1688 days agogithub.com - This tool extracts heterozygous kmer pairs from kmer count databases and performs gymnastics with them. We are able to disentangle genome structure by comparing the sum of kmer pair coverages (CovA + CovB) to their relative coverage (CovB / (CovA +...Bioinformatics Project Assistant at NITW
NATIONAL INSTITUTE OF TECHNOLOGY WARANGAL – 506 004 DEPARTMENT OF BIOTECHNOLOGY No. NITW/Bio/ Date: 30th March 2015 ADVERTISEMENT FOR PROJECT FELLOW (Research Staff) Applications are invited for the post of Project Fellow (Research...
