ArrayGen's focus on Genomics, NGS data analysis, custom array design, microarray data analysis thus cover a vast majority of Bioinformatics applications in the life sciences sector.
mrfast.sourceforge.net - mrFAST is a read mapper that is designed to map short reads to reference genome with a special emphasis on the discovery of structural variation and segmental duplications. mrFAST maps short reads with respect to user defined error threshold,...
Sr.Bioinformatics Analyst (NGS)
Experience Required: 3-5 years of experience
No of Positions : Multiple
Qualifications: Candidates with minimum qualification as M.Sc Bioinformatics with 3-5 years of experience in Life sciences R&D or...
hoffmann.bioinf.uni-leipzig.de - segemehl is a software to map short sequencer reads to reference genomes. Unlike other methods, segemehl is able to detect not only mismatches but also insertions and deletions. Furthermore, segemehl is not limited to a specific read length and is...
sourceforge.net - AccNET is a Perl application that presents a new way to study the accessory genome of a given set of organisms. Using the proteomes of these organisms, AccNET create a bipartite network compatible with common network analysis platforms. AccNET...
Postgraduate Institute of Medical Education and Research (PGIMER) - Chandigarh, Chandigarh
₹9,300 - ₹34,800 a month
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh invites Online Applications for recruitment of...
DuPont Industrial Biosciences has several summer internship positions
for undergrads available. We are looking for driven and creative interns
to conduct research in the following areas:
· Enzyme immobilization supports for select enzyme...
SLURM is a queue management system and stands for Simple Linux Utility for Resource Management. SLURM was developed at the Lawrence Livermore National Lab and currently runs some of the largest compute clusters in the world.
SLURM is similar in...
github.com - Hagfish is a tool that is to be used in data analysis of Next Generation Sequencing (NGS) experiments. Hagfish builds on the concept of coverage plots and aims to assist (amongst others) in quality control of de novo genome assembly or...
www.well.ox.ac.uk - Stampy is a package for the mapping of short reads from illumina sequencing machines onto a reference genome. It's recommended for most workflows, including those for genomic resequencing, RNA-Seq and Chip-seq. Stampy excels in the mapping of...