Jitendra Prajapati
A Bioinformatician
Our Sponsors
Related items
vcfR
By Archana Malhotra 3018 days agocran.r-project.org - Most variant calling pipelines result in files containing large quantities of variant information. The variant call format (vcf) is an increasingly popular format for this data. The format of these files and their content is discussed in...Ra assembler - a de novo DNA assembler for third generation sequencing data
By biogeek 2523 days agogithub.com - Integration of the Ra assembler - a de novo DNA assembler for third generation sequencing data developed on Faculty of Electrical Engineering and Computing (FER), Ruder Boskovic Institute (RBI) and Genome Institute of Singapore (GIS). Ra is in...Project Scientist at National Agri-Food Biotechnology Institute (NABI)
Advt. No. NABI/8(18)/2012-PME-3 Project Scientist recruitment in National Agri-Food Biotechnology Institute (NABI) Project Title : “Transfer and Evaluation of Indian Banana with Pro-Vitamin A (PVA) Constructs” Essential qualifications: Ph.D....AlignGraph: algorithm for secondary de novo genome assembly guided by closely related references
By Manisha Mishra 2412 days agogithub.com - AlignGraph is a software that extends and joins contigs or scaffolds by reassembling them with help provided by a reference genome of a closely related organism. Using AlignGraph AlignGraph --read1 reads_1.fa --read2 reads_2.fa --contig contigs.fa...Useful Bioinformatics Tools
By Poonam Mahapatra 3009 days ago Comments (1)molbiol-tools.ca - Collections of few handy tools for bioinformatician http://molbiol-tools.ca/Convert.htmEAGLER: a scaffolding tool for long reads.
By Jit 2365 days agogithub.com - EAGLER is a scaffolding tool for long reads. The scaffolder takes as input a draft genome created by any NGS assembler and a set of long reads. The long reads are used to extend the contigs present in the NGS draft and possibly join overlapping...Artemis Comparison Tool (ACT)
By Shruti Paniwala 3000 days agowww.sanger.ac.uk - ACT is a Java application for displaying pairwise comparisons between two or more DNA sequences. It can be used to identify and analyse regions of similarity and difference between genomes and to explore conservation of synteny, in the context of...SWALO: Scaffolding with assembly likelihood optimization
By Jit 2349 days agoatifrahman.github.io - SWALO (scaffolding with assembly likelihood optimization) is a method for scaffolding based on likelihood of genome assemblies computed using generative models for sequencing. Please email your questions, comments, suggestions, and bug reports to...Traineeship/Studentship conducts University of Delhi (Gargi College)
Traineeship/Studentship cunducts University of Delhi (Gargi College) on purely temporary for a period of six months. Traineeship — 01 (one post) Essential Qualification: Post Graduate degree in Bioinformatics or any other branch of Life Sciences...Converting a VCF into a FASTA given some reference !
By Jit 2318 days agoconverting a VCF file into a FASTA file given a reference sequence
