Jit
Enthusiast computational biologist with business dream !!!
Our Sponsors
Related items
Rosalind Problem Solution with Perl
Last updated 3925 days ago by JitRosalind is a platform for learning bioinformatics and programming through problem solving. Take a tour to get the hang of how Rosalind works. Bioinformatics Textbook Track Find more about Rosalind puzzle at...BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2698 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...Research Associate MANIT - Allahabad, Uttar Pradesh
Applications are invited from Indian nationals for the post of Research Assistant (on contract) in research project entitled “Identification of novel drug targets in Aspergillus fumigatus genome prioritized by essentiality based screening and...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2594 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...Research Associate at International Centre for Genetic Engineering and Biotechnology (ICGEB)
Research Associate International Centre for Genetic Engineering and Biotechnology (ICGEB) Address: Aruna Asaf Ali Marg, Jawaharlal Nehru University, New Delhi Postal Code: 110067 City: New Delhi State: Delhi Qualifications: Experience in many...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 2243 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...Research Associate Bioinformatics job position in Indian Agricultural Statistics Research Institute...
Research Associate Statistics Eligibility : M Phil / Phd, MSc Location : Delhi Last Date : 27 Jun 2015 Hiring Process : Walk - In Indian Agricultural Statistics Research Institute (IASRI) - Job DetailsDate of posting:03 Jun...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 2211 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...ICGEB Bioinformatics Research Associate Vacancy
Research Associate Position at ICGEB, New Delhi with Dr. Amit Sharma Starting 15th July 2015, the position relates to a project specifically for in silico drug docking, screening, design, optimisation and linkage with active chemists....FiNGS: Filters for Next Generation Sequencing
By Neel 1836 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...
