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Scientist Eligibility : MSc, M Phil / Phd, BE/B.Tech Location : Delhi Last Date : 08 Mar 2016 Hiring Process : Walk - In Regional Medical Research Centre - Notification Order No.1-51/Proj/RMRC/PB/ Scientist – II (Post Code:...

github.com - This software is designed to identify both simple and complex rearrangements from paired-end sequencing data. Users could ran it easily by just alling SVelter.py with proper parameters. It's also possible to ran it on multiple cores by...

Vacancy Notice PU/TS/01-16 JRF jobs in International Centre for Genetic Engineering and Biotechnology Area of research: Computational analysis of protein-protein interactions and metabolic reconstruction of pathways Qualification : Suitable...

Commercial tools Strand NGS offers many different tools including alignment, RNA-Seq, DNA-Seq, ChIP-Seq, Small RNA-Seq, Genome Browser, visualizations, Biological Interpretation, etc. Supports workflows “one can import the sample data in...

Jhpiego is a non-profit global health leader and Johns Hopkins University affiliate that is saving lives, improving health, and transforming futures. We partner with governments, health experts, and local communities to build the skills and systems...

easyfig.sourceforge.net - Easyfig has moved to github, for newer releases of Easyfig please visit our new webpage - https://mjsull.github.io/Easyfig.  Easyfig is a Python application for creating linear comparison figures of multiple genomic loci with an easy-to-use...

Research Fellow Bioinformatics Eligibility : BSc(Bio-Tech), MSc(Bio-Tech) Location : Ludhiana Last Date : 19 Apr 2016 Hiring Process : Walk - In Punjab Agricultural University Research Fellow Bioinformatics job opportunities in Punjab...

bioen-compbio.bioen.illinois.edu - Rreference-Assisted Chromosome Assembly (RACA), an algorithm to reliably order and orient sequence scaffolds generated by NGS and assemblers into longer chromosomal fragments using comparative genome information and paired-end...

genomebiology.biomedcentral.com - REAPR is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads, without the use of a reference genome for comparison. It can be used in any stage of an assembly pipeline to automatically break incorrect scaffolds and...

www.usadellab.org - Paired End: java -jar trimmomatic-0.35.jar PE -phred33 input_forward.fq.gz input_reverse.fq.gz output_forward_paired.fq.gz output_forward_unpaired.fq.gz output_reverse_paired.fq.gz output_reverse_unpaired.fq.gz ILLUMINACLIP:TruSeq3-PE.fa:2:30:10...