Rahul Agarwal
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Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By Rahul Nayak 2440 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...Java utilities for Next Generation Sequencing by Pierre Lindenbaum
By Robert M Willioms 4195 days agogithub.com - Java utilities for Bioinformatics https://github.com/lindenb/jvarkitngs-bits - Short-read sequencing tools
By Neel 2245 days agogithub.com - Binaries of ngs-bits are available via Bioconda. Alternatively, ngs-bits can be built from sources: Binaries for Linux/macOS From sources for Linux/macOS From sources for WindowsKAU Thrissur Biotech/Bioinformatics RA/SRF/JRF/Trainee/Studentships
Applications are invited from eligible candidates for the following posts at Bioinformatics Centre (DIC), IT- BT Complex, College of Horticulture, Kerala Agricultural University, Vellanikkara, Thrissur. 1. Research Associate Emoluments*:...HASLR: a tool for rapid genome assembly of long sequencing reads
By LEGE 2231 days agogithub.com - HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires long reads generated by Third Generation Sequencing technologies (such as PacBio or Oxford Nanopore) together with Next Generation...FACULTY POSITION at NATIONAL INSTITUTE OF TECHNOLOGY, ROURKELA
NIT, Rourkela, an institute of national importance under Ministry of HRD, Govt. of India invites applications from Indian nationals possessing excellent academic background along with commitment to quality teaching and research for faculty positions...Parliament2: Runs a combination of tools to generate structural variant calls on whole-genome...
By Jit 2112 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...Software developed in pevsner lab
By Robert M Willioms 4174 days agopevsnerlab.kennedykrieger.org - DRAGON: Database Referencing of Array Genes Online SNOMAD: Standardization and Normalization of Microarray Data SNPduo: SNP Analysis Between Two Individuals SNPtrio: Analyzing and Visualizing and Inheritance Patterns in Trios SNPscan: Data...Smudgeplot: Inference of ploidy and heterozygosity structure using whole genome sequencing data
By Neel 1475 days agogithub.com - This tool extracts heterozygous kmer pairs from kmer count databases and performs gymnastics with them. We are able to disentangle genome structure by comparing the sum of kmer pair coverages (CovA + CovB) to their relative coverage (CovB / (CovA +...Research Fellows at CSIR - Institute of Himalayan Bioresource Technology, Palampur, Himachal...
CSIR - Institute of Himalayan Bioresource Technology 2 vacancies of Project Fellow Name of the Post: Project Fellow No. of the Post: 02 Two Salary: Rs. 12000/- per month or Rs. 14000/- per month Age Limit: Max. 28 years as on 10.06.2015...
