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FinisherSC:a repeat-aware tool for upgrading de novo assembly using long reads
By Jit 2968 days agogithub.com - Here is the command to run the tool: python finisherSC.py destinedFolder mummerPath If you are running on server computer and would like to use multiple threads, then the following commands can generate 20 threads to run FinisherSC. python...Walk in interview for Research Associate, Studentship and Traineeship at BIF, NEHU, Tura Campus
BIOINFORMATICS INFRASTRUCTURE FACILITY (BIF) Department of RDAP North-Eastern Hil University, Tura Campus Tura-79402, Meghalaya Walk in interview for Research Associate, Studentship and Traineeship at BIF Applications are invited for the...LoRMA: A tool for correcting sequencing errors in long reads
By Abhimanyu Singh 2951 days agogite.lirmm.fr - An error correction method that uses long reads only. The method consists of two phases: first, we use an iterative alignment-free correction method based on de Bruijn graphs with increasing length of k-mers, and second, the corrected reads are...Assistant Professor at GAUHATI UNIVERSITY, GUWAHATI
Advt. No.T/2014/4 Ref. No. GU/Estt/T/308(VI)/2014/6451-61 Applications are invited from the Indian citizens for five (5) teaching posts of Assistant Professor (Contractual) under various departments of Gauhati University. Details of the...Rainbow: an integrated tool for efficient clustering and assembling RAD-seq reads
By Rahul Nayak 2908 days agosourceforge.net - Rainbow is developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. First, Rainbow clusters reads using a spaced seed method. Then, Rainbow implements a heterozygote calling like...China University of Macau PhD Position 2015 in Bioinformatics, Computer Science
The Computational Biology and Bioinformatics Group at the University of Macau is inviting applications for PhD Position. Applicants will work on a research project focusing on the flexible receptor protein-ligand docking algorithms for...Genome assembly tutorial "Genome Assembly for short and long reads"
By Jit 2816 days ago Comments (1)bioinformaticsdotca.github.io - In this lab we will perform de novo genome assembly of a bacterial genome. You will be guided through the genome assembly starting with data quality control, through to building contigs and analysis of the results. At the end of the lab you will...JNU Neuroscience/Systems Biology/Mathematical modeling JRF Vacancies
School of Computational and Integrative Sciences Jawaharlal Nehru University New Delhi 110067 Recruitment for Project Applications were invited from the citizens of India for filling up the following temporary position for the CSIR sponsored...SViper: Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact...
By Neel 2479 days agogithub.com - Call sviper ~$ ./sviper -s short-reads.bam -l long-reads.bam -r ref.fa -c variants.vcf -o polished_variants This will output a polished_variants.vcf file, that contains all the refined variants. Sometimes it is helpful to look at the...Rcorrector: efficient and accurate error correction for Illumina RNA-seq reads
By BioStar 2434 days agogithub.com - Rcorrector has an accuracy higher than or comparable to existing methods, including the only other method (SEECER) designed for RNA-seq reads, and is more time and memory efficient. With a 5 GB memory footprint for 100 million reads, it can be run...
