BOL

github.com - NucDiff locates and categorizes differences between two closely related nucleotide sequences. It is able to deal with very fragmented genomes, structural rearrangements and various local differences. These features make NucDiff to be perfectly...

Research Associate Bioinformatics recruitment in ICGEB, New Delhi Project :“Genetic Transformation and Development of Elite Transgenic Maize (Zea mays L.) for Biotic and Abiotic Stresses Tolerance”. Qualification: Ph.D. degree...

Senior Manager (Bioinformatics Operations) Rajiv Gandhi Centre for Biotechnology (RGCB) - Thiruvananthapuram, Kerala ₹15,600 - ₹39,100 a month Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications for the following positions from...

Advt. No. NABI/8(18)/2012-PME-3 Project Scientist recruitment in National Agri-Food Biotechnology Institute (NABI) Project Title : “Transfer and Evaluation of Indian Banana with Pro-Vitamin A (PVA) Constructs” Essential qualifications: Ph.D....

github.com - Integration of the Ra assembler - a de novo DNA assembler for third generation sequencing data developed on Faculty of Electrical Engineering and Computing (FER), Ruder Boskovic Institute (RBI) and Genome Institute of Singapore (GIS). Ra is in...

Chittaranjan National Cancer Institute Advertisement No.497/2016 Invites Applications For Senior Scientific Officer, Gr. II Note: Experience in the following field required: Molecular cancer cytogenetic and genetic toxicology Molecular drug...

atifrahman.github.io - SWALO (scaffolding with assembly likelihood optimization) is a method for scaffolding based on likelihood of genome assemblies computed using generative models for sequencing. Please email your questions, comments, suggestions, and bug reports to...

github.com - MEGAHIT is a single node assembler for large and complex metagenomics NGS reads, such as soil. It makes use of succinct de Bruijn graph (SdBG) to achieve low memory assembly. MEGAHIT can optionally utilize a CUDA-enabled GPU to...

mathgen.stats.ox.ac.uk - IMPUTE2 is a computer program for phasing observed genotypes and imputing missing genotypes. Most people use just a couple of the program's basic functions, but we have also built up a collection of specialized and powerful options. If you are...

github.com - NxRepair is a python module that automatically detects large structural errors in de novo assemblies using Nextera mate pair reads. The decector will break a contig at the site of an identified misassembly and will generate a new fasta file...