amos.sourceforge.net - Genome sequencing remains an inexact science, and genome sequences can contain significant errors if they are not carefully examined. Hawkeye is our new visual analytics tool for genome assemblies, designed to aid in identifying and correcting...
University of Padova (URL: http://protein.bio.unipd.it/)
A research fellowship is available at the BioComputing Laboratory, University of Padova (URL: http://protein.bio.unipd.it/). A highly motivated and creative candidate is sought to work on...
www.nature.com - Validated a widely accessible approach that can be used to establish functional causality for noncoding sequence variants identified by GWASs.
https://www.nature.com/articles/nm.3975
Contract Faculty-Bioinformatics at Maulana Azad National Institute of Technology
Job Description:F.No.11/10(1)/929 Qualifications: Candidates should have Ph.D. degree. If Ph.D. candidates are not available at least Post Graduate degree with...
Yau Group are a new research group based at the Wellcome Trust Centre for Human Genetics and the Department of Statistics at the University of Oxford.
Yau Group develops statistical and computational methods for the analysis of genomic datasets...
ADVERTISEMENT No. PR-54/2013
No. of Posts and Specialization: 1(UR)
Educational Qualification:
(i) Good academic record with a Ph.D. Degree in the concerned /allied /relevant disciplines.
(ii) The Ph.D. Degree shall be a mandatory...
doc-openbio.readthedocs.io - SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its...
NATIONAL INSTITUTE OF TECHNOLOGY CALICUT, KERALA
NOTIFICATION FOR FACULTY RECRUITMENT – 2013
(Faculty openings in Technology, Science, Architecture and Management at NIT Calicut, Kerala)
National Institute of Technology Calicut, Kerala,...
github.com - KAD is designed for evaluating the accuracy of nucleotide base quality of genome assemblies. Briefly, abundance of k-mers are quantified for both sequencing reads and assembly sequences. Comparison of the two values results in a single value per...