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BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2275 days agogithub.com - new de novo assembler called BASE. It enhances the classic seed-extension approach by indexing the reads efficiently to generate adaptive seeds that have high probability to appear uniquely in the genome. Such seeds form the basis for BASE...RA Bioinformatics at IISR
Bioinformatics Research Associate at Indian Institute of Spice Research Pay Scale: Rs. 40,000/-per month +HRA (as admissible) for Ph.D. holders and Rs. 38,000/-p.m. + HRA (as admissible) for Master degree holder Qualifications: a)Essential...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2171 days agogithub.com - nQuire implements a set of commands to estimate ploidy level of individuals from species, where recent polyploidization occurred and intraspecific ploidy variation is observed. Specifically, nQuire uses next-generation sequencing data to distinguish...Bioinformatics Project Assistant at Vector Control Research Centre (VCRC), Puducherry.
Applications are invited upto 27.07.2015 for filling up of one post of Project Assistant (UNRESERVED) to work under ICMR funded Non-Institutional adhoc project entitled “Biomedical Informatics centre’s of ICMR” at Vector Control Research Centre...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 1821 days agogithub.com - ClinCNV detects CNVs in germline and somatic context in NGS data (targeted and whole-genome). We work in cohorts, so it makes sense to try ClinCNV if you have more than 10 samples (recommended amount - 40 since we estimate variances from...Bioinformatics Scientist at NIN
No.NIN/PERS/Sch-88/2015-16/ WALK-IN-INTERVIEW (EMPLOYMENT NOTIFICATION) Eligible candidates are invited to apply for the following post on the ad hoc research project entitled “Biomedical Informatics Centre’s of ICMR” - funded by ICMR at this...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 1788 days agocsb5.github.io - LoFreq* (i.e. LoFreq version 2) is a fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data. It makes full use of base-call qualities and other sources of errors inherent in sequencing (e.g. mapping or...Five key traits to seek out in potential bioinformatics candidates !!!
By Jit 3441 days agoOnce your research group is ready to make a larger investment and hire a bioinformatician to gain a competitive edge, there are several key traits to seek out in potential candidates. The best bioinformatician are:-FiNGS: Filters for Next Generation Sequencing
By Neel 1414 days agogithub.com - Key features Filters SNVs from any variant caller to remove false positives Calculates metrics based on BAM files and provides filtering not possible with other tools Fully user-configurable filtering (including which filters to use and their...JRF in Bioinformatics @ Central University of Rajasthan
Central University of Rajasthan Department of Biotechnology School of Life Sciences Bandarsindri, Distt. Ajmer Applications are invited for one JRF position supported by DST sponsored project in Bioinformatics with Dr. Tarun Kumar...
