Jit
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Senior Manager (Bioinformatics Operations) at RGCB, India
No. RGCB/ADVT/ADMN&TECH/01/2016 August 17, 2016 RGCB invites applications for the following positions from Indian citizens with prescribed qualifications. Full details including job description, additional desirable qualifications, etc....Comparison of Short Read De Novo Alignment Algorithms
By Rahul Agarwal 4581 days agobiochem218.stanford.edu - Excellent article to introduce different sequencing methods along with tools for de novo assembly of sequencing reads and their relevant references. Title: Comparison of Short Read De Novo Alignment Algorithms Author: Nikhil GopalGenome STRiP
By Neel 3470 days agosoftware.broadinstitute.org - Genome STRiP (Genome STRucture In Populations) is a suite of tools for discovering and genotyping structural variations using sequencing data. The methods are designed to detect shared variation using data from multiple individuals.Genome STRiP...coursera genome assembly tutorial
By Jit 3024 days agogithub.com - Solutions to Coursera Genome Sequencing (Bioinformatics II)WALK-IN INTERVIEW @ JIPMER
Department of Preventive and Social Medicine , JIPMER, Puducherry –605006 WALK-IN INTERVIEW JIP/PSM/INDO-US TB/ 2016/ Walk-in-interview for the following vacant posts funded by Department of Biotechnology, Govt.of India for the project...COPE: an accurate k-mer-based pair-end reads connection tool to facilitate genome assembly
By Jit 3014 days agoftp.genomics.org.cn - An efficient tool called Connecting Overlapped Pair-End (COPE) reads, to connect overlapping pair-end reads using k-mer frequencies. We evaluated our tool on 30× simulated pair-end reads from Arabidopsis thaliana with 1% base error. COPE...JRF Bioinformatics at MANIT, India
Advt. No.: Maths./577/2016 Date: 12/08/2016 JRF Bioinformatics Job Position in Maulana Azad National Institute of Technology (MANIT) purely temporary basis Project Title : “Computational Approach to Study Complex Biological Network of Diseases...3d-dna: 3D de novo assembly (3D DNA) pipeline
By Jit 2991 days agogithub.com - This code is designed to enable anyone to reproduce the Hs2-HiC and the AaegL4 genomes reported in: Dudchenko et al., De novo assembly of the Aedes aegypti genome using Hi-C yields chromosome-length scaffolds. Science, 2017. Unless otherwise...vcfR
By Archana Malhotra 3487 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...ALPACA: A hybrid strategy for assembly of genomic DNA shotgun sequencing reads.
By Seema Singh 2868 days agogithub.com - ALPACA requires Celera Assembler 8.3 or later. It is recommended to build Celera Assembler from source. (Why? The pre-built binaries CA_8.3rc1 and CA8.3rc2 will work for any large data set. Detail paper...
