Poonam Mahapatra
Bioinformatics Researcher
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gapFinisher: A reliable gap filling pipeline for SSPACE-LongRead scaffolder output
By Rahul Nayak 2333 days agogithub.com - gapFinisher is based on the controlled use of a previously published gap filling tool FGAP and works on all standard Linux/UNIX command lines. They compare the performance of gapFinisher against two other published gap filling tools PBJelly and...Research Associate Bioinformatics Central Institute for Research on Buffaloes (CIRB) - Hisar,...
Research Associate (RA) under Network Project on Agricultural Bioinformatics Name of the Project : Network Project on Agricultural Bioinformatics Number of positions One Qualifications : Ph.D Degree in Bioinformatics/Biotechnology/...Parliament2: Runs a combination of tools to generate structural variant calls on whole-genome...
By Jit 2208 days agogithub.com - Parliament2 identifies structural variants in a given sample relative to a reference genome. These structural variants cover large deletion events that are called as Deletions of a region, Insertions of a sequence into a region, Duplications of a...RA Bioinformatics at TEZPUR UNIVERSITY
Walk-in-interview will be held on 23 February, 2015 at 11.00 a.m. for the following temporary positions in the DBT (U-EXCEL) sponsored project entitled “Sequencing genomes of some bacteria that invade/resides in tomato plant” under the Principal...Project Associate-I | Project Associate-II | Senior Project Associate @ IGIB
Experience in Next Generation Sequencing (NGS) application and interest in Genomics/ Clinical / Translational Applications. OR Good computational programming skills and deep interest in working on interface of Genomics and Clinical application....RA WALK-IN-INTERVIEW @ ACTREC
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Be proficient in LINUX, know perl or python, understand biology and Next Generation Sequencing. The intern will port Agile Assay Design pipelines into Galaxy. The intern will also learn to develope his/her own bioinformatics pipelines for PCR or...VariantBam: Filtering and profiling of next-generational sequencing data using region-specific rules
By Rahul Nayak 2810 days agogithub.com - VariantBam is a tool to extract/count specific sets of sequencing reads from next-generational sequencing files. To save money, disk space and I/O, one may not want to store an entire BAM on disk. In many cases, it would be more efficient to store...JRF Bioinformatics @ IISR, Kozhikode
JRF Bioinformatics Jobs recruitment in Indian Institute of Spices Research on temporary basis Name of the Scheme : Distributed Information Sub Centre – DISC Qualifications : M.Sc/ B Tech in Bioinformatics with NET/GATE or M Tech in...
