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Research opening @ IBAB, Bengaluru
Applications are invited for the position of Project Assistant in Bio-IT centre at IBAB, Electronic city, Bengaluru. The successful candidate will work in the next-generation sequencing (NGS) facility to perform nucleic acid isolations, quality and...Simka and SimkaMin are comparative metagenomics method dedicated to NGS datasets
By Neel 2439 days agogithub.com - Simka is a de novo comparative metagenomics tool. Simka represents each dataset as a k-mer spectrum and compute several classical ecological distances between them. Developper: Gaëtan Benoit, PhD, former member of...Scientist-B (Bioinformatics) at AIIMS, Delhi
Name of the Project: “Artificial intelligence in Oncology, Harnessing big data and advanced computing to provide personalized diagnosis and treatment for Cancer patients” Age Limit: 35 How to Apply for the AIIMS Life Science Job: Interested...Post Doc Computational Biology, Bioinformatics - Network Biology & Data Science, NGS (m/f/d)
https://www.jobvector.de/jobs-stellenangebote/biologie-life-sciences/forschung-entwicklung/post-doc-computational-biology-bioinformatics-network-biology-data-science-ngs-129867.html?suid=e522e9793b41817e52ac58d6963b94e2519920df Requirements Docto...10 NGS services companies around the globe !
By BioStar 1934 days agoAccording to the research report published, the top companies in NGS Services Market have new service launches, acquisitions, collaborations, partnerships, and also have expansions taken place in the NGS services space.Understanding HiFi Reads !
By Rahul Nayak 1447 days agopacb.com - While little public data is available for either of the new synthetic long read approaches, Illumina showed an example comparison earlier this year at the Festival of Genomics & Biodata conference (FoG 2022). In the IGV screenshot...Pacasus: Correction of palindromes in long reads from PacBio and Nanopore
By BioStar 2676 days agogithub.com - Tool for detecting and cleaning PacBio / Nanopore long reads after whole genome amplification. Check the poster from the Revolutionizing Next-Generation Sequencing (2nd edition) conference in the source...Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 2234 days agogithub.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...Pacman
By Rahul Nayak 4040 days agoThe pacman package is an R package management tool that combines the functionality of base library related functions into intuitively named functions.
