Jit
Enthusiast computational biologist with business dream !!!
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RA Bioinformatics at Institution: Centre for Human Genetics, Bangalore
Institution: Centre for Human Genetics, Bangalore Discipline: Molecular Genetics of Human Disease Biology Minimum qualification: MSc in any branch of life sciences Applications are invited for the position of a Research Assistant in the...nanofilt: Filtering and trimming of long read sequencing data
By Jit 2779 days ago Comments (1)github.com - Filtering on quality and/or read length, and optional trimming after passing filters.Reads from stdin, writes to stdout. Intended to be used: directly after fastq extraction prior to mapping in a stream between extraction and...BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2699 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...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2595 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 PhD / PostDoc / Job Rejection
By Jit 3904 days ago Comments (1)While your PhD or PostDoc application, it is more common that you got rejected by many professors. Don't disappoint reply it calmly.ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 2244 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...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 2212 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...Research Associate, Project Fellow (Biological Sciences) at IGIB
Research Associate, Project Fellow (Biological Sciences) Institute of Genomics & Integrative Biology (IGIB) - New Delhi, Delhi Pay Scale: Rs. 22,000/- + 30 % HRA per month Educational Requirements: PhD in any branch of Biological Sciences...FiNGS: Filters for Next Generation Sequencing
By Neel 1837 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...
