The question at http://rosalind.info/problems/1d/
Script are moved to http://bioinformaticsonline.com/snippets/view/34633/clump-finding-problem-solved-with-perl
Live Webinar on RNA-Seq Data Analysis
Abstract: Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical...
fragment size: the Illumina WGS protocol generates paired-end reads from both ends of longer fragments. The lengths of these fragments are assumed to be sampled from a normal distribution. Therefore, in the absence of structural variants,...
Research Scientist Jobs opportunity in University of Delhi on temporary basis
Qualifications : Ph. D.
Desirable : Experience on DNA Markers, plant genome mapping and bioinformatics
No. of Post : 03
Department : Genetics
Salary : Rs....
github.com - Mix is a tool that combines two or more draft assemblies, without relying on a reference genome and has the goal to reduce contig fragmentation and thus speed-up genome finishing. The proposed algorithm builds an extension graph where vertices...
github.com - HALC, a high throughput algorithm for long read error correction. HALC aligns the long reads to short read contigs from the same species with a relatively low identity requirement so that a long read region can be aligned to at least one contig...
National Facility for Marine Cyanobacteria
Department of Marine Biotechnology
Bharathidasan University
Tiruchirappalli -620024, Tamil Nadu
Applications are invited from individuals who have high motivation to do research for the below...
github.com - nQuire provides a statistical framework to study organisms with intraspecific variation in ploidy. nQuire is likely to be useful in epidemiological studies of pathogens, artificial selection experiments, and for historical or ancient samples where...