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LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 2308 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...Postdoctoral Researcher at Department of Biotechnology, Catholic University of Daegu, Kyungsan,...
Applications are invited from Indian nationals for a Post Doctoral position at Molecular Medical Laboratory, Department of Biotechnology, Catholic University of Daegu, Kyungsan, Kyungbuk, South Korea. Qualification required: PhD in Life Sciences/...FiNGS: Filters for Next Generation Sequencing
By Neel 1934 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...Research Associate NBFGR - Lucknow, Uttar Pradesh
NBFGR, Lucknow is recruiting Bioinformatics experts for the post of Research Associate Name of Position : Research Associate No of Post : One Desired candidate Profile : Candidate should be PhD in Bioinformatics or equivalent or Post-Graduation...
Libraries or management tools for high throughput sequencing data
Last updated 619 days ago by LEGEGATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.These methods enable the analysis of data sets of any size on multi-core desktop...RA Bioinformatics at IISER
Advertisement: Research Position in Computational Biology in the group of Shree P. Pandey Positions available in the area of NGS data analysis, bioinformatics, plant genomics Project Description: Projects involves high throughput analysis of data...Qualimap2: Evaluating next generation sequencing alignment data
By Jit 2833 days agoqualimap.bioinfo.cipf.es - Qualimap 2 is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data and its derivatives like...RA Bioinformatics at North Eastern Hill University
Bioinformatics Infrastructure Facility, Department of RDAP, NEHU vacancy of Research Associate Name of the Post: Research Associate No. of the Post: 01 One Age Limit: Max. 35 years Salary: Rs. 22000/- per month plus HRA Required Job...Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By BioJoker 2630 days agogithub.com - Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The...Pacman
By Rahul Nayak 4136 days agoThe pacman package is an R package management tool that combines the functionality of base library related functions into intuitively named functions.
