BOL

github.com - gapFinisher is based on the controlled use of a previously published gap filling tool FGAP and works on all standard Linux/UNIX command lines. They compare the performance of gapFinisher against two other published gap filling tools PBJelly and...

Registration for BINC examination 2015 will open soon.

github.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...

Department of Botany & Bioinformatics Centre NORTH-EASTERN HILL UNIVERSITY, SHILLONG 793022 Applications with complete bio-data from candidates possessing the required qualifications are invited for the posts of JRF (2) and Project Assistant...

Experience in Next Generation Sequencing (NGS) application and interest in Genomics/ Clinical / Translational Applications. OR Good computational programming skills and deep interest in working on interface of Genomics and Clinical application....

20th International BioInformatics Workshop on Virus Evolution and Molecular Epidemiology (VEME) 9 - 14 August 2015 St. Augustine, Trinidad and Tobago Organiser: Christine Carrington (University of the West Indies - UWI, St. Augustine, Trinidad...

Shanghai, China-headquartered pharmatech company WuXi (NYSE: WX) has acquired NextCODE Health, a genomic analysis and bioinformatics company based in the USA.

github.com - VariantBam is a tool to extract/count specific sets of sequencing reads from next-generational sequencing files. To save money, disk space and I/O, one may not want to store an entire BAM on disk. In many cases, it would be more efficient to store...

Recruitment The following posts are to be filled purely on temporary basis under CIBA Component of “Centre for Agricultural Bioinformatics (CABin)” project at this Institute. Posts Research Associate Date & Time of Interview 18th Feb 2015...

github.com - jackalope simply and efficiently simulates (i) variants from reference genomes and (ii) reads from both Illumina and Pacific Biosciences (PacBio) platforms. It can either read reference genomes from FASTA files or simulate new ones. Genomic variants...