Jit
Enthusiast computational biologist with business dream !!!
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nanofilt: Filtering and trimming of long read sequencing data
By Jit 2993 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...Bioinformatics Faculty at BHARATHIDASAN UNIVERSITY
BHARATHIDASAN UNIVERSITY (Reaccredited by NAAC with ‘A’ grade) TIRUCHIRAPPALLI - 620 024 I N V I T E S APPLICATIONS FOR FACULTY POSITIONS UNDER UGC XII PLAN CREATED POSTS ON CONTRACTUAL BASIS TILL 31.03.2017 IN THE FOLLOWING UNIVERSITY...BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2912 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...R.A Bioinformatics at JNU, Delhi
R.A Jobs opportunity in Jawaharlal Nehru University (JNU) on purely temporary basis Project Title : "Structural and functional characterization of serine biosynthetic pathway enzymes from Entamoeba histolytica" No. of Post :...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2808 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 Trainees recruitment in National Agri-Food Biotechnology Institute (NABI)
Research Trainees recruitment in National Agri-Food Biotechnology Institute (NABI) Eligibility : Pursuing final year of M.Sc./M.Tech. Subject category for training : I. Agricultural biotechnology II. Computational biology and bioinformatics...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 2457 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...M. D. University, Rohtak is looking for the post of Research Associate
M. D. University, Rohtak - Rohtak, Haryana M. D. University, Rohtak is looking vacancies for the post of Research Associate Project entitled: "Establish of Bioinformatics Facility for biology teaching through bioinformatics" Name of post:...Scientist E-II or F in Bioinformatics & Computational Biology at Rajiv Gandhi Centre for...
Advt. No.RGCB Advt./SCI 2015/1 Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications for the following three faculty scientist positions: Scientist G in any of the following disciplines of disease biology: Cancer...FiNGS: Filters for Next Generation Sequencing
By Neel 2050 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...
