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LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 2210 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 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...FiNGS: Filters for Next Generation Sequencing
By Neel 1835 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...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....
Libraries or management tools for high throughput sequencing data
Last updated 520 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...Research Scientist at DuPONT
Research Scientist Hyderabad, Telangana Job Description Job Description The Global Trait Discovery Informatics (GTDI) group located at the DuPont Knowledge Centre (DKC), Hyderabad, India is currently seeking applications for a highly...Qualimap2: Evaluating next generation sequencing alignment data
By Jit 2735 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 at CSIR-URDIP
CSIR - UNIT FOR RESEARCH AND DEVELOPMENT OF INFORMATION PRODUCTS (CSIR- URDIP) Adv. No. URDIP/ 15/2015 Opportunity for young Bioinformatics Professionals to make a career in the area of Intellectual Property CSIR has set up a Unit for...Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By BioJoker 2531 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...Project Fellow at IHBT - Palampur, Himachal Pradesh
The Institute is working relentlessly on developing technologies for sustainable utilization of Himalayan bioresources, and in the area of tea, floriculture, bamboos and medicinal and aromatic plants. Looking at the mission of the Institute,the...
